Methods and compositions for treating conditions
Patent 7557088 Issued on July 7, 2009.
Estimated Expiration Date: 
March 28, 2027.
Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.
March 28, 2027.
Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.
Patent References
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Inventor
Assignee
ApplicationNo. 11692847 filed on 03/28/2007
US Classes:514/18 3 or 4 peptide repeating units in known peptide chain
ExaminersPrimary: Kosar, Andrew D
Attorney, Agent or Firm
Foreign Patent References
International ClassesA61K 38/07A61K 38/12
Description>BACKGROUNDThere are many conditions that affect plants and animals, including but not limited to pain, metabolic conditions/thermoregulation conditions (e.g., fever), pathogen infections, and neurological/neurodegenerative conditions (e.g., Alzheimer'sdisease). There is a significant need to identify new compositions and methods to treat and/or prevent such conditions. INCORPORATION BY REFERENCE All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to beincorporated by reference. SUMMARY OF THE INVENTION The invention herein involves compositions comprising, consisting essentially of, or consisting of a polypeptide of the invention or a homolog, analog, mimetic, salt, prodrug, metabolite, or fragment thereof or combination. In some embodiments,a polypeptide comprises, consists essentially of, or consists of one or more amino acid sequences selected from the group consisting of SEQ ID NOs: 1-349 or an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-244, 248-249, 257-349,or a reverse sequence of any of the above or of SEQ ID NOs: 1-244, 248-249, 257-279, or 306-349. For example, in some embodiments, a composition comprises a polypeptide having amino acid sequence of any one of SEQ ID NOs: 1-349 or of any one of SEQ ID NOs: 1-14 or 50-244, 248-249, 257-349, or of any one of SEQ ID NOs: 1, 2, 153, 304-349 orof any one of SEQ ID NOs: 1, 153, 304 or 305. In some embodiments, a composition comprises a polypeptide having an amino acid sequence which is the reverse of any one of SEQ ID NOs: 1-349 or any one of SEQ ID NOs: 1, 153, 304-349. The invention hereinalso contemplates homologs, analogs (especially small molecule analogs), mimetics, salts, prodrugs, metabolites, and fragments of the above polypeptides and compositions comprising the same. The compositions herein can be used to modulate, prevent, or treat pain, inflammation, infections (e.g., bacterial, fungal, viral, etc.), and metabolic processes or conditions in an organism (plant or animal). As such the compositions hereinexhibit both analgesic and anesthetic properties. Examples of metabolic conditions include, but are not limited to, pain, wound healing, fever, neurological and neurodegenerative conditions, heat production, inflammation, fever, homeothermy, breakdown of triglycerides, glycolysis, Krebs cycle,fermentation, photosynthesis, metabolic rate, biotic and abiotic stress, secretions, oxidative stress, stress, neoplastic growth, skin condition, cardiovascular conditions, neurological and neurodegenerative conditions, and mental and behavioraldisorders. Such processes or conditions can occur in a cell, group of cells, or an entire organism. The compositions herein can be used for modulating, preventing, and treating condition(s) in organisms. Such organisms can be animals and/or plants. In some embodiments, the compositions herein (e.g., a composition comprising a polypeptide of any one or more of SEQ ID NOs: 1-349 or of any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or of any one or more of SEQ ID NOs: 1, 153, 304-349)are used to modulate or treat pain, such as nociceptive (non-chronic) pain, neuropathic (chronic) pain, idiopathic pain, headaches, low back pain, cancer pain, arthritis pain, sprains, bone fractures, pain resulting from burns, pain associated withbumps, pain associated with bruises, inflammatory pain (e.g., from an infection or arthritic disorder), pain from obstructions, myofascial pain, pain from nerve trauma (e.g., dystrophy/causalgia), phantom limb pain, entrapment neuropathy (e.g., carpaltunnel syndrome), and peripheral neuropathy. Thus, in some cases a composition herein (e.g., comprising any one or more of SEQ ID NOs: 1-349 or SEQ ID NOs: 1, 153, 304-349 or an analog, salt metabolite, or prodrug thereof) is administered to an animal to treat pain. Such pain can benon-chronic pain, neuropathic pain, or idiopathic pain. It is further contemplated that a composition comprising a polypeptide described herein (e.g., SEQ ID NOs: 1, 153, 304-349) is co-administered with one or more other pain relief medications. Forexample, a polypeptide described herein, such as SEQ ID NOs: 1, 153, or 304-349 can be administered simultaneously with, co-formulated with, or administered in the same therapy as a pain reliever selected from the group consisting of small molecules(e.g., non-narcotic and narcotic analgesics) and peptide opioids. In some embodiments, the compositions herein (e.g., a composition comprising a polypeptide comprising, consisting essentially of, or consisting of any one or more of SEQ ID NOs: 1-349 or 1-244, 248-249, and 257-349, or SEQ ID NOs: 1 or 153 or 304or 305) are used to module or treat inflammatory conditions that may or may not cause pain. Such conditions may show one or more of the following symptoms: redness, heat, tenderness and swelling. Examples of such conditions include, but are not limitedto, chronic inflammatory diseases, such as rheumatoid arthritis, inflammatory bowel disease, systemic lupus erythematosus, multiple sclerosis, type I and II diabetes, asthma, and inflammatory diseases of the central nervous system such as multiplesclerosis, abscess, meningitis, encephalitis and vasculitis. In some embodiments, the compositions herein (e.g., a composition comprising a polypeptide comprising, consisting essentially of, or consisting of any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349 orany one or more of SEQ ID NOs: 1 or 153 or 304 or 305) are used to modulate or treat cardiovascular conditions. Examples of cardiovascular conditions associated with pain and/or inflammation include, but are not limited to, angina, arrhythmia, highblood pressure, stroke, congestive heart failure, atherosclerosis, peripheral artery diseases, high cholesterol levels, and heart attacks. In some embodiments, the compositions herein (e.g., a composition comprising a polypeptide comprising, consisting essentially of, or consisting of any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, orany one or more of SEQ ID NOs: 1 or 153 or 304 or 305) are used to modulate or treat fever or abnormal body temperature, whether or not such temperature is associated with pain. Examples of such conditions include infections. In some embodiments, the compositions herein (e.g., a composition comprising a polypeptide comprising, consisting essentially of, or consisting of any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, orany one or more of SEQ ID NOs: 1, 153 or 304 or 305) are used to modulate or treat a neurological or neurodegenerative condition or a mental or behavioral disorder. Examples of neurological conditions associated with pain and/or inflammation include,but are not limited to, Alzheimer's disease, amnesia, Aicardi syndrome, amyotrophic lateral sclerosis (Lou Gehrig's disease), anencephaly, anxiety, aphasia, arachnoiditis, Arnold Chiari malformation, attention deficit syndrome, autism, Batten disease,Bell's Palsy, bipolar syndrome, brachial plexus injury, brain injury, brain tumors, childhood depression, Charcot-Marie Tooth disease, depression, dystonia, dyslexia, encephalitis, epilepsy, essential tremor, Guillain-Barre syndrome, hydrocephalus,hyperhidrosis, Krabbes disease, learning disabilities, leukodystrophy, meningitis, Moebius syndrome, multiple sclerosis, muscular dystrophy, Parkinson's disease, peripheral neuropathy, obsessive-compulsive disorder, postural orthostatic tachycardiasyndrome, progressive supranuclear palsy, prosopagnosia, schizophrenia, shingles, Shy-Drager syndrome, spasmodic torticollis, spina bifida, spinal muscular atrophy, stiff man syndrome, synesthesia, syringomyelia, thoracic outlet syndrome, tourettesyndrome, toxoplasmosis, and trigeminal neurolagia. Examples of mental and behavioral disorders include, but are not limited to, anxiety disorder, panic disorder, obsessive-compulsive disorder, post-traumatic stress disorder, social phobia (or social anxiety disorder), specific phobias, andgeneralized anxiety disorder Any of the above conditions can also be accompanied by or manifested by other conditions such as depression, drug abuse, or alcoholism. In some embodiments, the compositions herein are used to treat fever that occurs with many different conditions such as inflammation and infectious diseases. In some embodiments, the compositions herein are used to modulate or treat neoplastic growth. Examples of neoplastic growth include, but are not limited to, breast cancer, skin cancer, bone cancer, prostate cancer, liver cancer, lung cancer,brain cancer, cancer of the larynx, gallbladder, pancreas, rectum, parathyroid, thyroid, adrenal, neural tissue, head and neck, colon, stomach, bronchi, kidneys, basal cell carcinoma, squamous cell carcinoma of both ulcerating and papillary type,metastatic skin carcinoma, osteosarcoma, Ewing's sarcoma, reticulum cell sarcoma, myeloma, giant cell tumor, small-cell lung tumor, gallstones, islet cell tumor, primary brain tumor, acute and chronic lymphocytic and granulocytic tumors, hairy-cellleukemia, adenoma, hyperplasia, medullary carcinoma, pheochromocytoma, mucosal neuromas, intestinal ganglioneuromas, hyperplastic corneal nerve tumor, marfanoid habitus tumor, Wilm's tumor, seminoma, ovarian tumor, leiomyoma tumor, cervical dysplasia andin situ carcinoma, neuroblastoma, retinoblastoma, soft tissue sarcoma, malignant carcinoid, topical skin lesion, mycosis fungoide, rhabdomyosarcoma, Kaposi's sarcoma, osteogenic and other sarcoma, malignant hypercalcemia, renal cell tumor, polycythermiavera, adenocarcinoma, glioblastoma multiforme, leukemias, lymphomas, malignant melanomas, epidermoid carcinomas, and other carcinomas and sarcomas. Thus, in some embodiments, a composition herein (e.g., a composition comprising any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 153 or 304 or 305) can be administered simultaneously with, co-formulated with, or administeredin the same therapy as an anti-neoplastic agent. In some embodiments, the compositions herein are used to modulate and treat abnormal temperature associated with non-rapid eye movement (NREM) during sleep, thermotaxis of human spermatozoa toward fertilization site (isthmic-ampullary junction)at ovulation, and hot flashes in postmenopausal women. The compositions herein can be used to treat addiction in an animal by administering to the animal any of the compositions described herein (e.g., peptides, small molecules, nucleic acids encoding the above, etc.). In some embodiments, the compositions herein are used to treat or prevent plants/crops from yield losses. Examples of plants that may be treated with the compositions herein include major crops (e.g., corn, soybeans, hay, wheat, cotton, sorghum,rice, etc.) Examples of conditions resulting in crop losses are diseases caused by bacteria, viruses, and fungi. Other examples of conditions that may result in crop losses that can be preventable or diminished by the compositions herein include stressconditions such as drought, freezing, oxidative stress, unfavorable or reduced temperatures, infection by pathogens and other unfavorable environmental conditions. In some embodiments, the compositions herein are used to modulate (e.g., increase, decrease or control) temperature. Examples of plants that may be treated with the compositions herein include ornamental crops: flower bulbs (e.g., Tulips,Daffodils, Hyacinths, Crocus, Dutch iris, Allium etc.), cut flowers (e.g., roses, carnation, lily, gladiolus, bird of paradise, etc); vegetable crop (e.g., tomato, cucumber, celery, eggplants, pumpkins, carrot, lettuce, zucchini, etc.); fruit crops(e.g., apple, citrus, peach, pear, plums, banana, pineapple, olive, avocado, papaya, mango, nuts, berries, and other types of agricultural crops such as grain (e.g., corn, soybeans, hay, wheat, barley, corn, cotton, sorghum, and rice) and trees used forlumber (e.g, Douglas fir, cedar, maple, oak, poplar). In some embodiments, the compositions herein are used to modulate (e.g., increase, decrease or control) seed production. Examples of plants that may be treated with the compositions herein include seeds of ornamental crops, vegetable crops,fruit and nut crops, seeds of other types of agricultural crops, or other plants disclosed herein In some embodiments, the compositions herein are used to modulate (e.g., increase, decrease or control) secretory products in plants or animals. Such secretary products include, but are not limited to, small volatiles and non-volatile compoundssuch as terpenes, fatty acid oxidative products, and amines, as well as high molecular weight molecules such as polypeptides and polysaccharides. Such secretions can be, for example, involved in inter-, intra-cellular communications and/or diseases. The invention herein also provides for nucleic acids that encode the compositions herein and nucleic acids that are complementary to nucleic acids that encode the compositions herein. Nucleic acids that encode the compositions herein can beinserted into a vector to express the polypeptides herein recombinantly. Nucleic acids that are complementary to the polypeptides herein can be used to modulate the expression of certain polypeptides and as diagnostics or research tools. The compositions herein can be formulated with one or more carriers or excipients for delivery to an organism, such as an animal or a plant. Such carriers can be, for example, pharmaceutical carriers, veterinary carriers, and agriculturalcarriers. For delivery to an animal, the compositions herein may be administered in a therapeutically effective dose to reduce, inhibit, eliminate, ameliorate or prevent a condition. Similarly, for delivery to a plant (e.g., a crop plant), thecompositions herein can be delivered in an effective dose to reduce, inhibit, eliminate, ameliorate or prevent a condition. The invention also provides for antibodies or antibody fragments that are specific to the polypeptides herein. Such antibodies or antibody fragments can be used therapeutically, prophylactically, or for research purposes. Such antibodies orantibody fragments are preferably humanized and/or monoclonal. The invention herein also provides for methods for screening for binding molecules (receptors) and for agents (ligand) that modulate the composition herein, or their binding to receptors. Binding affinity is determined by a competitive assayusing labeled agents (e.g., biotinylated or fluorescent) incubated with the receptors in the presence of various concentrations of a composition of the invention. The affinity binding constant, Ka, has to be of greater than or equal to about105 to 107 M-1, or greater than or equal to about 108 M-1, or greater than or equal to about 109 M-1 or greater than or equal to about 1010 M-1. In certain embodiments binding affinity constants of peptidesfor the binding polypeptides may exceed 1011 to 1012 M-1. Affinities of binding polypeptides for ligands according to the present invention can be readily determined using conventional techniques, for example those described by Scatchardet al. (1949 Ann. N.Y. Acad. Sci. 51:660), or by other various techniques described in the scientific literature. The invention herein also provides small molecules and/or peptidomimetics of the polypeptides herein and methods for making the same. In some aspects the invention herein contemplates methods of treating addiction in an animal by administering to the animal a composition comprising any of the compositions herein. The present invention also contemplates a method for treating a plant or an animal suffering from a condition comprising administering to said plant or animal a composition comprising a peptide selected from the group consisting of SEQ ID NOs:306-349 or a small molecule thereof. In some cases the condition described above can be pain, a neurodegenerative or neurological condition, an addiction, Alzheimer's disease, a pathogen infection, a metabolic disorder, fever, inflammation, orneoplastic growth. The present invention also relates to compositions comprising a peptide comprising, consisting essentially of, or consisting of SEQ ID NOs: 306-349 or a small molecule thereof as well as pharmaceutical excipients comprising the above compositionand a pharmaceutical excipient or an agricultural formulation comprising the composition above an agricultural excipient or a cosmetic formulation comprising the composition above with a cosmetic excipient, etc. In some cases, the composition (or formulation derived thereof) comprises, consists essentially of, or consists of a peptide comprising Phe-Leu, Leu-Phe, Pro-Ser, or Ser-Pro or a small molecule thereof. SUMMARY OF THE FIGURES FIG. 1 illustrates the efficacy of SEQ ID NO: 1 in relieving pain in rats 3 days after surgery. FIG. 2 illustrates the efficacy of SEQ ID NO: 1 in relieving pain in rats 3 h after surgery FIG. 3 illustrates the efficacy of SEQ ID NO: 1 in relieving pain in rats after surgery FIG. 4 illustrates heat production by Sauromatum guttatum appendix treated with aspirin (ASA) and various opioid peptides and the neurotoxic peptide β-amyloid peptide (Aβ 1-42). FIG. 5 illustrates heat production by Sauromatum guttatum appendix treated with salicylic acid (SA) in the presence of human opioid peptides (β-Endorphin and Neuropeptide AF) and, β-amyloid peptide, (Aβ 1-42); and a plant virulentbacterial pathogen (Pst DC3000). FIG. 6 illustrates heat production by Sauromatum guttatum appendix treated with 2,6-dihydroxybenzoic acid (2,6-DHBA) in the presence of β-amyloid peptide (Aβ 1-42), SEQ ID NO: 2, and SEQ ID NO: 1. FIG. 7 illustrates effects of SEQ ID NO: 1 on 3-hour post-surgical pain in rats. FIG. 8 illustrates effects of SEQ ID NO: 1 on 3-day post-surgical pain in rats. DETAILED DESCRIPTION OF INVENTION The present invention relates to compositions and methods for modulating conditions in plants and/or animals. Such conditions include mitochondrial related or metabolic related conditions, pain, plant pathogens, infections, fever, Alzheimer'sdisease, etc. In one aspect, a composition herein includes a polypeptide comprising, consisting essentially of, or consisting of any one or more of: SEQ ID NOs: 1-349, or any one or more of: SEQ ID NOs: 1-24, 50-244, 248-249, or 257-349, or any one or more of:SEQ ID NOs: 1-2, 153, or 304-349 or any one or more of SEQ ID NOs: 1 or 153 or 304 or 305. In one aspect, a composition comprises a nucleic acid sequence encoding one or more of the above. In one aspect, a composition comprises an antibody that specifically binds an epitope comprising one or more of the above polypeptides. In one aspect, the present invention relates to a method for identifying novel compositions (e.g., polypeptides, peptide nucleic acids, nucleic acids, and small molecules) that modulate conditions in plants or animals as described herein (e.g.,pain, fever, neurodegenerative conditions, metabolic conditions, etc.). Such methods include administering a test agent to a thermogenic plant; measuring the temperature of said thermogenic plant; and determining if said test agent modulates temperaturein said plant. In one aspect, the compositions herein are used to treat a mitochondrial or metabolic condition selected from the group consisting of: innate immune response activation and ability to fight parasites and pathogens, pain, inflammation, temperatureregulation, neoplastic growth (e.g., cancer), skin and dermatological conditions, and neurological and neurodegenerative conditions. DEFINITIONS The term "agonist" as used herein refers to any compound, small molecule, or agent, or a peptide that stimulates a biological activity. Examples of agonists include, but are not limited to, antibodies, antisense nucleic acids, siRNA nucleicacids, and other binding agents. Such agents can stimulate receptors, e.g., morphine antagonist of the opiate μ receptors. The term "amino acid" or "amino acid residue" refers to an amino acid, which is preferably in the L-isomeric form. When an amino acid residue is part of a polypeptide chain, the D-isomeric form of the amino acid can be substituted for theL-amino acid residue, as long as the desired functional property is retained. NH2 refers to the free amino group present at the amino terminus of a polypeptide. COOH refers to the free carboxyl group present at the carboxyl terminus of apolypeptide. The amino acids herein can be represented by their standard 1-letter code or 3-letter code. An amino acid residue represented by "X" or "Xxx" refers to any one of the naturally occurring or non-naturally occurring amino acid residues knownin the art or to a modification of a nearby residue. In keeping with standard protein nomenclature described in J. Biol. Chem., 1969, 247:3552-59, and adopted at 37 C.F.R. .sctn..sctn.1.821-2461.822, all amino acid residue sequences represented hereinby formulae have a left to right orientation in the conventional direction of amino-terminus to carboxyl-terminus. In addition, the phrase "amino acid residue" is broadly defined to include modified and unusual amino acids, such as those referred to in37 C.F.R. .sctn..sctn.1.821-1.822, and incorporated herein by reference. In a peptide or polypeptide, suitable conservative substitutions of amino acids are known to those of skill in this art and can be made generally without altering the biologicalactivity of the resulting molecule. Watson et al., (1987, Molecular Biology of the Gene, 4th Edition, The Benjamin Cummings Pub. Co., p. 224), is incorporated herein by reference. Amino acid substitutions are typically of single residues, suchsubstitutions are preferably made with those set forth in Table I, but may be of multiple residues, either clustered or dispersed. An amino acid can be replaced with a different naturally occurring or a non-conventional amino acid residue. Suchsubstitutions may be classified as "conservative", in which case an amino acid residue contained in a polypeptide is replaced with another naturally occurring amino acid of similar character either in relation to polarity, side chain functionality orsize. Additions encompass the addition of one or more naturally occurring or non-conventional amino acid residues. Deletion encompasses the deletion of one or more amino acid residues. TABLE-US-00001 TABLE I Conservative amino acid substitution Original residue Conservative substitution(s) Ala Gly; Ser Arg Lys Asn Gln; His Cys Ser Gln Asn Glu Asp Gly Ala; Pro His Asn; Gln Ile Leu; Val Leu Ile; Val Lys Arg; Gln; Glu Met Leu;Tyr, Ile Phe Met; Leu; Tyr Ser Thr Thr Ser Trp Tyr Tyr Trp; Phe Val Ile; Leu Substitutions encompassed by the present invention may also be "non-conservative", in which an amino acid residue which is present in a peptide is substituted with an amino acid having different properties, such as naturally-occurring amino acidfrom a different group (e.g., substituting a charged or hydrophobic amino acid with alanine), or alternatively, in which a naturally-occurring amino acid is substituted with a non-conventional amino acid. The term "analog(s)" as used herein refers to a composition that retains the same structure or function (e.g., binding to a receptor) as a polypeptide or nucleic acid herein, such as the same gene from a different organism. Examples of analogsinclude mimetics or peptidomimetics, peptide, nucleic acids, small and large organic or inorganic compounds, as well as derivatives and variants of a polypeptide or nucleic acid herein. Such derivatives and variants refer to peptides and nucleic acidsthat differ from the naturally occurring polypeptides and nucleic acids by one or more amino acid or nucleic acid deletions, additions, substitutions or side-chain modifications. In some embodiments, a peptide analog is a peptide in which one or more ofthe amino acids has undergone side-chain modifications. Examples of side-chain modifications contemplated by the present invention include modifications of amino groups such as by reductive alkylation by reaction with an aldehyde followed by reductionwith NaBH4; amidination with methylacetimidate; acylation with acetic anhydride; carbamoylation of amino groups with cyanate; trinitrobenzylation of amino groups with 2,4,6-trinitrobenzene sulphonic acid (TNBS); acylation of amino groups withsuccinic anhydride and tetrahydrophthalic anhydride; and pyridoxylation of lysine with pyridoxal-5-phosphate followed by reduction with NaBH4. In some embodiments, a peptide analog is one in which the guanidine group of arginine residue(s) ismodified by the formation of heterocyclic condensation products with reagents such as 2,3-butanedione, phenylglyoxal and glyoxal; carboxyl group(s) is modified by carbodiimide activation via O-acylisourea formation followed by subsequent derivitisation,for example, to a corresponding amide; sulphydryl group(s) may be modified by methods such as carboxymethylation with iodoacetic acid or iodoacetamide; performic acid oxidation to cysteic acid; formation of a mixed disulphides with other thiol compounds;reaction with maleimide, maleic anhydride or other substituted maleimide; formation of mercurial derivatives using 4-chloromercuribenzoate, 4-chloromercuriphenylsulphonic acid, phenylmercury chloride, 2-chloromercuri-4-nitrophenol and other mercurials;carbamoylation with cyanate at alkaline pH. In any of the analogs herein, any modification of cysteine residues preferably does not affect the ability of the peptide to form the necessary disulphide bonds. In some embodiments, a peptide analogcomprises tryptophan residue(s) that are modified by, for example, oxidation with N-bromosuccinimide or alkylation of the indole ring with 2-hydroxy-5-nitrobenzyl bromide or sulphenyl halides; tyrosine residues altered by nitration with tetranitromethaneto form a 3-nitrotyrosine derivative; imidazole ring(s) of a histidine residue modification accomplished by alkylation with iodoacetic acid derivatives or N-carbethoxylation with diethylpyrocarbonate; proline residue(s) modified by, for example,hydroxylation in the 4-position; glycosylation variants from a completely unglycosylated molecule to a modified glycosylated molecule; and altered glycosylation patterns as a result from expression of recombinant molecules in different host cells. The term "antagonist" as used herein refers to any compound, small molecule, or agent, a peptide that inhibits or reduces a biological activity. Examples of antagonist molecules include, but are not limited to, peptides, small molecules,antibodies, antisense nucleic acids, siRNA nucleic acids, and other binding agents. The term "antibody" is used in the broadest sense and specifically covers, for example, polyclonal antibodies, monoclonal antibodies (mAbs) (including agonist, antagonist, and neutralizing antibodies), chimeric antibodies, antibody compositionswith mono and polyepitopic specificity, single chain antibodies, anti-idiotypic (anti-Id) antibodies to antibodies that can be labeled in soluble or bound form, polymers and conjugates of immunoglobulins, as well as fragments, regions or derivativesthereof (e.g., separate heavy chains, light chains, Fab, F(ab')2, Fabc, and Fv). Antibody fragments can be prepared for example by enzymatic cleavage of antibodies with enzymes such as pepsin or papain. Antibody aggregates, polymers and conjugates canbe generated by diverse methods, e.g. by thermal treatment, reaction with substances such as glutaraldehyde, reaction with immunoglobulin-binding molecules, biotinylation of antibodies and subsequent reaction with streptavidin or avidin. The term"monoclonal antibody" as used herein refers to an antibody obtained from a population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical except for possible naturally-occurring mutations thatmay be present in minor amounts. The term "antigen" includes monovalent and polyvalent antigens. A polyvalent antigen is a molecule or a molecule complex to which simultaneous binding of more than one immunoglobulin is possible, whereas a monovalent antigen can bind only asingle antibody at each particular time. Hapten is normally the designation given to a molecule which is not immunogenic per se but which is normally bound to a carrier for immunization purposes. The term "effective amount" as used herein when referring to a composition means the amount or dosage of that composition that is required to induce a desired effect. In some embodiments, an effective dose refers to an amount that is required toinduce a local analgesic, anti-pyrogenic, flowering, pesticide, anti-dementia, and/or anti-inflammatory effect. The term "fragment" as used herein refers to a portion of a composition. For example, when referring to a polypeptide, a fragment of a polypeptide is some but not the entire amino acid polymer that comprises the polypeptide. A polypeptidefragment can have up to 99, 95, 90, 85, 80, 75, 70, 65, or 60% of the sequence of the parent polypeptide. In some embodiments, a fragment has between 3-40, 3-30, 4-20, or 4-10 amino acids of the parent sequence. The terms "gene therapy" and "genetic therapy" refer to the transfer of heterologous nucleic acids to the certain cells, target cells, of a mammal, particularly a human, with a disorder or conditions for which such therapy is sought. The nucleicacid is introduced into the selected target cells in a manner such that the heterologous DNA is expressed and a therapeutic product encoded thereby is produced. Alternatively, the heterologous nucleic acids can in some manner mediate expression of anucleic acid that encodes the therapeutic product; it can encode a product such as a peptide or RNA that in some manner mediates, directly or indirectly, expression of a therapeutic product. Genetic therapy can also be used to nucleic acid encoding agene product replace a defective gene or supplement a gene product produced by the mammal or the cell in which it is introduced. The term "homolog" when referring to a polymer (e.g., a peptide or a nucleic acid) refers to a second polymer that has at least about 50 sequence identity, at least 55% sequence identity, at least 60% sequence identity, at least 65% sequenceidentity, at least 70% sequence identity, at least 80% sequence identity; or at least about 81% sequence identity, at least about 82% sequence identity, or at least about 83% sequence identity, or at least about 84% sequence identity, or at least about85% sequence identity, or at least about 86% sequence identity, or at least about 87% sequence identity, or at least about 88% sequence identity, or at least about 89% sequence identity, or at least about 90% sequence identity, or at least about 91%sequence identity, or at least about 92% sequence identity, or at least about 93% sequence identity, or at least about 94% sequence identity, or at least about 95% sequence identity or at least about 96% sequence identity, or at least about 97% sequenceidentity, or at least about 98% sequence identity or at least about 99% sequence identity and preferably the same function. For example, a polypeptide homologous to any of the polypeptides herein (e.g., SEQ ID NOs: 1-349) is one that can have at least80% sequence identity and similar function of modulating pain or fever, or more preferably acting as an agonist or antagonist for pain receptors. The term "isolated" means altered from its natural state; i.e., if it occurs in nature, it has been changed or removed from its original environment, or both. For example, a naturally occurring polynucleotide or a polypeptide naturally presentin a living animal in its natural state is not "isolated", but the same polynucleotide or polypeptide separated from the coexisting materials of its natural state is "isolated", as the term is employed herein. For example, with respect topolynucleotides, the term isolated means that it is separated from the nucleic acid and cell in which it naturally occurs. The term "protein", "peptide", "oligopeptides" or "polypeptide" as used herein refers to any composition that includes two or more amino acids joined together by a peptide bond. For the sake of clarity, the use of any of the above terms isinterchangeable unless otherwise specified. It will be appreciated that polypeptides (or peptides or proteins or oligopeptides) often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids, andthat many amino acids, including the terminal amino acids, may be modified in a given polypeptide, either by natural processes such as glycosylation and other post-translational modifications, or by chemical modification techniques which are well knownin the art. Among the known modifications which may be present in polypeptides of the present invention include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of a flavanoid or a heme moiety, covalentattachment of a polynucleotide or polynucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphatidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalentcross-links, formation of cystine, formation of pyroglutamate, formylation, gamma-carboxylation, glycation, glycosylation, glycosylphosphatidyl inositol (GPI) membrane anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation,proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to polypeptides such as arginylation, and ubiquitination. The term "protein" also includes "artificial proteins"which refers to linear or non-linear polypeptides, consisting of alternating repeats of a peptide (e.g., any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1, 153, or 304-349), and a spacer. A DNA-construct encoding the peptide and aspacer alternate repeats can be synthesized using methods known in the art (Rotzschke et al., 1997, Proc. Natl. Acad. Sci. USA 94:14642-14647). The above methods allow for the amplification of the antigenicity of the peptide and for insertion intoan expression vector at high levels. The term "opioid" as used herein means all agonists and antagonists of opioid receptors, such as mu (μ), kappa (κ), and delta (δ) opioid receptors and subtypes thereof. For a discussion of opioid receptors and subtypes see Goodmanand Gilman's The Pharmacological Basis of Therapeutics 9th ed. J. G. Harman and L. E. Limird Eds., McGraw-Hill New York, 1996, pp. 521-555, which is incorporated herein by reference for all purposes. The opioid can be any opioid receptor agonist orantagonist known or to be developed. Preferred opioids interact with the μ-opioid receptor or the κ- and ε-opioid receptors. Preferably, the opioid is an opioid-receptor agonist or antagonist. The term "organism" as used herein can be, for example, a microorganism (e.g., virus or bacteria), plant (e.g., crop plants such as soy, wheat, barley, rice, corn, sugar, etc.), or animal. Animals include both mammals (e.g., farm animals,donkeys, goats, rabbits, dogs, cats, swine, cattle, sheep, horses, or primates) and non-mammals, (e.g., insects and birds, including chickens). In some cases the animal is a mammal, or a human. The term "purified" as used herein to describe a polypeptide, polynucleotide, or other compositions, refers to such polypeptide, polynucleotide, or other composition separated from one or more compounds, which are usually associated with it innature. Such other compositions can be, for example, other polypeptides or polynucleotides, carbohydrates, lipids, etc. The term "purified" can also be used to specify the separation of monomeric polypeptides of the invention from oligomeric forms suchas homo- or hetero-dimers, trimers, etc. The term "purified" may also be used to specify the separation of covalently closed (i.e. circular) polynucleotides from linear polynucleotides. A substantially pure polypeptide or polynucleotide typicallycomprises at least about 50%, 60%, 70%, 80%, or 90% weight/weight of a polypeptide or polynucleotide sample, or at least about 95%, 96%, 97%, 98%, 99%, or 99.5% weight/weight of a polypeptide or polynucleotide sample. As a preferred embodiment, apolypeptide or polynucleotide of the present invention is at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 96%, 96%, 98%, 99%, or 100% pure relative to heterologous polypeptides and polynucleotides, respectively. Compositions The compositions herein can include any one or more of the polypeptides, nucleic acids, antibodies, or small molecules described herein or any homolog, analog, prodrug, metabolite, salt, or polymorph thereof. The polymorphs contemplated hereinare preferably the most stable crystalline form of the composition. For example, the polymorph may be water-soluble. Polymorphs of any of the compositions herein can be detected using any method know in the art such as in vitro testing, where thematerial is crystallized by different methods. Once a crystal is created, its water solubility is determined and the most thermodynamically stable polymorph is selected. In some embodiments, the invention herein contemplates improving, alleviating, preventing or treating a condition in a plant, wherein the condition is associated with metabolism, heat production, or pathogen resistance by modulating (e.g., byexpressing recombinantly or otherwise, or by inhibiting or antagonizing) any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1, 153, 304-349; or by modulating any one or more of SEQ ID NOs: 245, 246, 247, 253 or any fragment thereofor complex thereof or a protein or complex comprising SEQ ID NOs: 245, 246, 247, 253. The present invention also contemplates alleviating, preventing or treating a condition in a plant by administering to the plant a composition comprising any one ormore of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1, 153, or 304-349 or a nucleic acid encoding the same, or an antibody that selectively bind the above, or a small molecule that mimics any of the above or a polymorph of any of the above. Thecondition of the plant can be, for example, one that is associated with metabolism, heat production, or pathogen resistance. In some embodiments, the invention herein contemplates improving, alleviating, preventing or treating a condition in an animal, such as a human, wherein the condition can be, e.g., pain, fever, Alzheimer's disease, or a metabolic condition, or inplants, wherein the condition can be, e.g., temperature, resistance to pathogen, and a metabolic condition, by modulating (e.g., using gene therapy, selectively binding using antibodies) antagonizing, or administering as a therapeutic a compositioncomprising any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-24, 50-152, 248-250, 254-349, or any one or more of SEQ ID NOs: 1, 153, 304-349 or any fragment thereof, or complex thereof, or a polymorph of any of the above or asmall molecule equivalent to any of the above. (For example, polypeptides such as SEQ ID NO: 250 and all other peptides described herein from human can be genetically engineered into a vector and transplanted into plants.) A polypeptide herein can further comprise additional amino acid residues in its C-terminus and/or N-terminus For example, the present invention contemplates any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1, 153, 304-349further comprising one or more amino acids such as, e.g., KFLPS (SEQ ID NO: 257), FLPSI (SEQ ID NO: 258), RFLPS (SEQ ID NO: 259) or FLPSE (SEQ ID NO: 260). Thus, a polypeptide herein can be a 2-mer (e.g., Lys-Pro, Pro-Lys, Phe-Lys, Lys-Phe, Ser-Ser,Pro-Ser, Ser-Pro, Ser-Leu), a 3-mer (e.g., part of any of the polypeptides herein, such as the middle portion thereof), 4-mer, 5-mer, 6-mer, 7-mer, 8-mer, 9-mer, 10-mer, 11-mer, 12-mer, 13-mer, 14-mer, 15-mer, or larger, and may be up to 40, 30, 20, or10 amino acids long. In some cases, the reverse sequences of any of the polypeptides herein can be used. In alternative or in addition to the above, any of the polypeptides herein can comprise one or more D-amino acids. For example, polypeptides of the inventioninclude those comprising, consisting essentially of, or consisting of: any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1, 153, 304-349; or any one or more of SEQ ID NOs: 1-152, 245-256, or 257-349, wherein at least one of theamino acids is a D-amino acid. In some cases the D-amino acids are the first 2 amino acids from the N-terminus. In some cases, the D-amino acids are the first three amino acids from the N-terminus. In some cases all of the amino acids are D-aminoacids. In some embodiments, a composition comprises a polypeptide comprising, consisting essentially of, or consisting of any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-14, 50-152, 248-249, 257-349, or any one or more of SEQID NOs: 1, 2, 153, 304-349, or any homolog, analog, prodrug, metabolite, or fragment thereof, or any salt thereof, small molecule thereof, nucleic acid encoding thereof, antibody thereof, or polymorph thereof. In some embodiments, the compositions herein include a polypeptide having the reverse amino acid sequence of any of the above amino acid sequences, such as e.g., SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 153-244, or 280-349 or ahomolog, analog, prodrug, metabolite, or fragment therefor salt thereof, or small molecule that mimics any of the above, or a nucleic acid encoding any of the above, or antibody that selectively binds any of the above, or a polymorph of any of the above. In some embodiments, the compositions herein include a peptide having the reverse amino acid sequence of any of the above amino acid sequences, such as SEQ ID NOs: 245-247 or any homolog, analog, prodrug, metabolite, or fragment thereof, or anysalt thereof, small molecule thereof, nucleic acid encoding thereof, antibody thereof, or polymorph thereof. For example, a composition herein can comprise a peptide fragment of SEQ ID NOs: 245, 246, and/or 247 which is between 3-50, 3-40, 3-30, 3-20,or 3-10 amino acids in length. In some cases, such fragments can have at least one or at least two phenylalanines. In some cases, such peptide fragments can comprise the sequence Phe-Leu-Pro-Ser (SEQ ID NO: 1). Any of the peptides herein arecontemplated in both their forward and reverse sequences. SEQ ID NOs: 152-244, 280-298, are the reverse sequences of SEQ ID NOs: 1-14 and 50-151, 257-279. In another aspect, the present invention relates to nucleic acids that encode any of the above peptides and antibody that specifically bind any of the above polypeptides. In some embodiments, the compositions (e.g., polypeptides) herein are used to modulate the effects of SEQ ID NO: 49 or to reduce the effects or treat or prevent Alzheimer's disease. In some embodiments, the above compositions (e.g., polypeptides) can be used modulate or enhance the effects of SEQ ID NOs: 1548, 248-249. In some embodiments, the above compositions (e.g., polypeptides) can be used to create a library to analyze functionality of compounds and compositions (e.g., small molecules) that regulate mitochondria activities. In some embodiments, a composition herein comprises a small molecule that mimics (e.g., has similar 3D structure or has similar biological activity) as any of the polypeptides herein. In some embodiments, a composition herein comprises a polymorph of any of the polypeptides or small molecules herein. In some embodiments, the compositions herein comprise a salt of any of the above. In some embodiments, the above compositions (e.g., peptides) can be used for screening antagonists, agonists, and modulators of different mitochondrial activities. 1. Polypeptides In some aspects a composition herein comprises, consists essentially of, or consists of one or more of the polypeptides described herein such as those that comprise, consist essentially of, or consist of any one of amino acid sequences of any oneor more of SEQ ID NOs: 1-349 or an analog, salt, polymorph, metabolite, or prodrug thereof or any one or more of SEQ ID NOs: 1-244, 248-249, or 257-349 or an analog, salt, polymorph, metabolite, or prodrug thereof; or sequences which are the reverse ofthe above or a homolog, analog, salt, prodrug, fragment, or metabolite of the above, or a polymorph of any of the above, or a combination thereof. In some cases, a composition herein comprises a polypeptide comprising any one or more of SEQ ID NOs: 1-349. In some cases such polypeptide has up to 10,000, 1,000, 100, 90, 80, 70, 60, 50, 40, 30, 20, 10, 9, 8, 7, 6, 5, 4, or 3 amino acids. The invention herein also contemplates analogs, salts, polymorphs, metabolites, or prodrugs thereof. In some cases, a composition comprises of a polypeptide that consists essentially of any one or more of SEQ ID NOs: 1-349. In some cases such polypeptide has up to 10,000, 1,000, 100, 90, 80, 70, 60, 50, 40, 30, 20, 10, 9, 8, 7, 6, 5, 4, or 3amino acids. The invention herein also contemplates analogs, salts, polymorphs, metabolites, or prodrugs thereof. In some cases, a composition comprises of a polypeptide that consists of any one or more of SEQ ID NOs: 1-349. In some cases such polypeptide has up to 10,000, 1,000, 100, 90, 80, 70, 60, 50, 40, 30, 20, 10, 9, 8, 7, 6, 5, 4, or 3 amino acids. The invention herein also contemplates analogs, salts, polymorphs, metabolites, or prodrugs thereof. In some cases, a composition includes more than 1, 2, 3, 4, 5, or 6 of the polypeptides described herein or an analog, salt, polymorph, metabolite, or prodrug thereof. The invention herein also contemplates compositions comprising peptides such as Leu-Pro and Pro-Leu (e.g., Xxx-Leu-Pro, Xxx-Pro-Leu, Leu-Pro-Xxx, Pro-Leu-Xxx, Xxx-Leu-Pro-Xxx, and Xxx-Pro-Leu-Xxx, as well as longer peptides comprising any of theabove sequences). In such embodiments, Xxx can be Phe, Ser, Trp, Tyr, or Pro, for example. Other peptides contemplated herein include: Phe-Leu, Leu-Phe, Pro-Ser, or Ser-Pro and peptides that comprise or consist essentially of any of the above. For example, the invention herein can comprise, consist essentially of, or consist of a peptide comprising dipeptide Pro-Leu conservative substitution dipeptide thereof, or a homolog, derivative, or analog thereof, or a small molecule thereof, ora salt, metabolite, or prodrug thereof, or a nucleic acid encoding such peptide; and a pharmaceutical excipient. The present invention also contemplates a composition comprising, consisting, or consisting essentially of: a peptide comprising Xxx-Leu-Pro or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof,or a nucleic acid encoding such peptide; and a pharmaceutical excipient. In some cases, Xxx is an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution ofany of the above, or an analog or a derivative of any of the above. The present invention also contemplates a composition comprising, consisting, or consisting essentially of: a peptide comprising Xxx-Leu-Phe or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof,or a nucleic acid encoding such peptide; and a pharmaceutical excipient. In some cases, Xxx is an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution ofany of the above, or an analog or a derivative of any of the above. The present invention also contemplates a composition comprising, consisting, or consisting essentially of: a peptide comprising Leu-Pro-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof,or a nucleic acid encoding such peptide; and a pharmaceutical excipient. In some cases Xxx is an amino acid such as Tyr, Thr, Glu, Asp or Ser or a conservative substitution of any of the above, or an analog or a derivative of any of the above. The present invention also contemplates a composition comprising, consisting, or consisting essentially of: a peptide comprising Ser-Leu-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof,or a nucleic acid encoding such peptide; and a pharmaceutical excipient. In some cases, Xxx is an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution ofany of the above, or an analog or a derivative of any of the above. The present invention also contemplates a composition comprising, consisting, or consisting essentially of: a peptide comprising Xxx-Leu-Pro-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrugthereof, or a nucleic acid encoding such peptide; and a pharmaceutical excipient. In some cases, each of Xxx can be Tyr or Phe or Trp or His or Pro or an analog or a derivative thereof. In some cases, each of Xxx can be Phe or Ser or a conservativesubstitution of any of the above, or an analog or a derivative of any of the above. The present invention also contemplates a composition comprising, consisting, or consisting essentially of: a peptide comprising Xxx-Pro-Leu-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrugthereof, or a nucleic acid encoding such peptide; and a pharmaceutical excipient. In some cases, each of Xxx can be Tyr or Phe or Trp or His or Pro or an analog or a derivative thereof. In some cases, each of Xxx can be an aromatic amino acid or aderivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution of any of the above, or an analog or a derivative of any of the above. In some cases, Xxx is Ser or a conservativesubstitution of Ser, or an analog or a derivative of Ser. The present invention also specifically contemplates pharmaceutical formulation comprising a composition comprising, consisting, or consisting essentially of tripeptides such as: Phe-Leu-Pro (SEQ ID NO: 344), Trp-Leu-Prp, Tyr-Leu-Pro, Pro-leu-Phe(SEQ ID NO: 346), Pro-Leu-Trp, and Pro-Leu-Tyr. Any of the above amino acids can be substituted by a conservative substitution, or an analog or derivative of any of the above. The invention also contemplates non-linear (e.g., cyclic) forms of the aboveand small molecules equivalent to any of the above. In any of the embodiments described herein a composition (e.g., peptide) can be linear or non-linear (e.g., cyclic). Thus, any one of SEQ ID NOS: 1-349 can be made cyclical. Examples of cyclical peptides contemplated include:cyclo(Xxx-Leu-Pro-Ser), wherein Xxx can be any amino acid or wherein Xxx is Phe, Pro, Ser, Tyr, Trp or H is, cyclo (Phe-Leu-Pro-Ser) (SEQ ID NO: 1), cyclo(Tyr-Leu-Pro-Ser) (SEQ ID NO: 350), cyclo (Trp-Leu-pro-Ser) (SEQ ID NO: 351), cyclo(Ser-Pro-Leu-Phe)(SEQ ID NO: 153), cyclo(Ser-Pro-Leu-Tyr) (SEQ ID NO: 352), and cyclo(Ser-Pro-leu-Trp) (SEQ ID NO: 353). Thus, a composition herein can comprise, consist, or consist essentially of a cyclic peptide (e.g., a cyclic peptide of any of the peptides hereinsuch as SEQ ID NO: 1-349) or an analog (e.g., small molecule) thereof or salt, prodrug, or metabolite thereof. In some cases, a composition comprises a non-linear (e.g., cyclic) peptide of SEQ ID NO: 1, 153, 304-349 or an analog thereof. Methods forforming cyclic peptides are known to those skilled in the art. Any of the peptides described herein can have one or more amino acids replaced by another naturally occurring or non-naturally occurring amino acid, preferably having similar charge, 3D structure, or by a conservative substitutions. Any of the peptides herein can further be modified by one or more of the following modifications: acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of a flavanoid or a heme moiety, covalent attachment of a polynucleotide orpolynucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphatidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cystine,formation of pyroglutamate, formylation, gamma-carboxylation, glycation, glycosylation, glycosylphosphatidyl inositol (GPI) membrane anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing,phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to polypeptides such as arginylation, and ubiquitination. Furthermore, any of the peptides herein can have one or more D-amino acids or one or more L-amino acids. In some cases, a peptide has at least 1, 2, 3, 4, or 5 D-amino acids or at least 1, 2, 3, 4, or 5 L-amino acids. As further described herein, compositions herein include those comprising any of the above peptides and small molecules equivalent thereof and homologs and analogs thereof, and polymorphs thereof, and fragments thereof, as well as prodrugs,metabolites and salts thereof. Such compositions can be used to treat or prevent a condition in a plant or an animal. In some cases, such compositions are used to treat a condition in a human. Such a condition can be e.g., pain, a neurological orneurodegenerative condition (e.g., Alzeimer's), inflammation, addiction, a metabolic disorder, neoplastic growth, or fever. In some cases, such compositions are used to treat a plant infected by a pathogen or to prevent infection of a plant by apathogen. In some embodiments, a composition comprises more than 1, 2, 3, 4, and 5 of the polypeptides above. The polypeptides herein may be created synthetically by any means known in the art (synthetically synthesized or using recombinant DNA technology). In some embodiments, they may include an additional methionine at the N-terminus (e.g., SEQ IDNO: 105, MFAGYFAG) or an N-terminus methionine may be included on to them. In some embodiments, a polypeptide herein has up to about 100, 95, 90, 85, 80, 75, 70, 65, 60, 55, 50, 45, 40, 35, 30, 25, 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, or 4 amino acids residue; or at least about 3, 4, 5, 6, 7, 8, 9,10, 11, 12, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, or 50, amino acid residues; or between about 2-50, 2-40, 2-30 or 2-10 amino acid residues. In some embodiments, a polypeptide herein has up to 500,000, 100,000, 75,000, 50,000, 15,000,14,000, 13,000, 12,000, 11,000, 10,000, 9,000, 8,000, 7,000, 6,000, 5,000, 4,000, 3,000, 2,000, 1,000, 900, 800, 700, 600, 500, 400, 300, or 200 Daltons. In some embodiments, a polypeptide herein has between 200-200,000, 300-100,000, 400-50,000, or500-1000 Daltons. The polypeptides herein are preferably isolated such that it is free of other compounds or molecules that it normally is associated with in vivo. For example, an isolated peptide of the invention can constitute at least about 50%, about 55%,about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 99% w/w of a sample containing it. In some embodiments, a polypeptide of the invention is purified. In some embodiments, a polypeptide of the present invention can be present in different conformational states (e.g., extended, single β-bend, and double β-bend (Deschamps, 2005)). The design of potent and selective opioid peptides andsmall analgesic drugs have involved the application of both conformational and topographical constraints (e.g., unsubstituted Gly 3 residue in of enkephalin can be replaced with d-Ala, or mercaptoproline, 21 or removing the Gly 3 residue to form a morerigid cyclic tetrapeptide (Deschamps, 2005, AAPS J. 7:E813; Hashimoto et al., 2002, Bioorg. Med. Chem. 10:3319; Salvadorii et al., 2002, BBRC, 223:640). In some embodiments, a polypeptide of the present invention present in different oligomerization states as a result of formulation in saline and other formulations required for bioactivity e.g., aggregations of beta-amyloid peptide (Murphy 2002),or self assembly of peptides (Ulrich et al., 1999). Polypeptides in different oligomerization states (or not oligomerized) can be used as backbone for cyclization and modification to constrain the conformation state of the bioactive peptide. In some embodiments, a polypeptide herein is modifiedor adapted for slow-release. Such modification can include substitution of one or more, 2 or more, 3 or more, or 4 or more amino acids residues from an L-amino acid residue to a D-amino acid residue. In some embodiments at least about 10%, 20%, 30%,40%, 50%, 60%, 70%, 80%, 90% or 100% of the residue in a polypeptide are D-amino acids. In some embodiments, a polypeptide of the present invention includes one or more post-translational modifications, e.g., N-linked or O-linked carbohydrate chains, processing of N-terminal or C-terminal ends, attachments of chemical moieties tothe amino acid backbone, chemical modifications of N-linked or O-linked carbohydrate chains, and addition or deletion of an N-terminal methionine residue as a result of prokaryotic host cell expression. The polypeptides may also be modified with adetectable label, such as an enzymatic, fluorescent, isotopic or affinity label to allow for detection and isolation of the polypeptide. Also provided by the invention are chemically modified derivatives of the polypeptides of the invention, which may provide additional advantages such as increased solubility, stability and circulating time of the polypeptide, or decreasedimmunogenicity. See U.S. Pat. No. 4,179,337. The chemical moieties for derivitization may be selected. See, U.S. Pat. No. 4,179,337, which is hereby incorporated by reference in its entirety. The chemical moieties for derivitization may beselected from water-soluble polymers such as polyethylene glycol (PEG), copolymers, carboxymethylcellulose, dextran, polyvinyl alcohol and the like. Such derivitization may occur at random positions within the molecule, or at predetermined positionswithin the molecule and may include one, two, three or more attached chemical moieties. For example, in some embodiments the chemical moiety used for derivitization may be a polymer of any molecular weight, and may be branched or unbranched. If PEG is used for derivitization, the preferred molecular weight is between about 1 kDaand about 100 kDa (the term "about" indicating that in preparations of PEG, some molecules will weigh more, some less, than the stated molecular weight) for ease in handling and manufacturing. Other sizes may be used, depending on the desiredtherapeutic profile (e.g., the duration of sustained release desired, the effects, if any on biological activity, the ease in handling, the degree or lack of antigenicity and other known effects of the PEG to a therapeutic polypeptide or analog). The PEG molecules (or other chemical moieties) should be attached to the polypeptide with consideration of effects on functional or antigenic domains of the polypeptide. There are a number of attachment methods available to those skilled in theart, e.g., EP 0 401 384, (coupling PEG to Granulocyte Colony Stimulating Factor (G-CSF)), Malik et al., (1992), Exp. Hematol. 20:1028-1035. This article reports on pegylation of Granulocyte/Macrophage Colony Stimulating Factor (GM-CSF) using tresylchloride, and its disclosure is hereby incorporated by reference in its entirety. For example, PEG may be covalently bound through amino acid residues via a reactive group, such as, a free amino or carboxyl group. Reactive groups are those to which anactivated PEG molecule may be bound. The amino acid residues having a free amino group may include lysine residues and the N-terminal amino acid residues; those having a free carboxyl group may include aspartic acid residues glutamic acid residues andthe C-terminal amino acid residue. Sulfhydryl groups may also be used as a reactive group for attaching the PEG molecules. Preferred for therapeutic purposes is attachment at an amino group, such as attachment at the N-terminus or lysine group. The polypeptides herein can be chemically modified at the N-terminus. Using PEG as an illustration of the present composition, one may select from a variety of PEG molecules (by molecular weight, branching, etc.), the proportion of PEG moleculesto polypeptide (polypeptide) molecules in the reaction mix, the type of pegylation reaction to be performed, and the method of obtaining the selected N-terminally pegylated polypeptide. The method of obtaining the N-terminally pegylated preparation(i.e., separating this moiety from other monopegylated moieties if necessary) may be by purification of the N-terminally pegylated material from a population of pegylated polypeptide molecules. Selective polypeptides chemically modified at theN-terminus modification may be accomplished by reductive alkylation, which exploits differential reactivity of different types of primary amino groups (lysine versus the N-terminal) available for derivitization in a particular polypeptide. Under theappropriate reaction conditions, substantially selective derivitization of the polypeptide at the N-terminus with a carbonyl group containing polymer is achieved. In any of the embodiments herein, a polypeptide of the present invention may be modified in its N-terminus. Examples of N-terminus modifications include an N-terminus methionine, N-terminus signal peptide, or a prosequence. An N-terminusmethionine may be used for expression of a polypeptide recombinantly. A "signal sequence" or "presequence" refers to any sequence of amino acids bound to the N-terminal portion of a polypeptide herein (e.g., an amino acid sequence selected from SEQ IDNOs: 1-349, or any homolog or analog thereof), which may participate in the secretion of the polypeptide. The term "prosequence" as used herein refers to a sequence of amino acids bound to the mature form of a polypeptide herein (e.g., an amino acidsequence selected from the group consisting of SEQ ID NOs: 1-349, or any homolog or analog thereof), which when removed results in the appearance of the "mature" form of the polypeptide (e.g., an amino acid sequence selected from the group consisting ofSEQ ID NOs: 1-349, or any homolog or analog thereof). Preferably, a prosequence is autocleaved/cleaved by naturally occurring enzymes, which are found at an area in which the mature polypeptide needs to be active. In some embodiments a polypeptide herein includes one or more conservative substitutions. Such substitutions are selected from the Table I. Other known conserved substitutions may also be known to a person of ordinary skill in the art. In some embodiments, a polypeptide of the present invention is modified to be more resistant to proteolysis. For example, a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence of (or encoded by) any one ormore of SEQ ID NOs: 1-349, (any of the above with a methionine at the N-terminus) or any homolog, analog or fragment thereof may include one or more peptide bonds in which the --CONH-- peptide bond is modified and replaced by a non-cleavable bond, e.g. a(CH2NH) reduced bond, a (NHCO) retro inverso bond, a (CH2--O) methylene-oxy bond, a (CH2--S) thiomethylene bond, a (CH2CH.sub.2) carba bond, a (CO--CH2) cetomethylene bond, a (CHOH--CH2) hydroxyethylene bond), a (N--N)bound, a E-alkene bond or also a --H--CH-- double bond. In some embodiments, a polypeptide sequence herein is constructed in its reverse sequence to prevent degradation. Examples of reverse sequence include those of SEQ ID NOs: 153-244, 280-298. In any of the embodiments herein, the peptides or polypeptides can be oligomerized. For example, the present invention contemplates homodimers and heterodimers of the peptides herein (e.g., a homodimer, homotrimer, or homotetramer of SEQ ID NOs:1 or 153 or a heterodimer, heterotrimer, or homotetramer of SEQ ID NOs: 1 and 153). 2. Nucleic Acids The present invention also provides for a nucleic acid that encodes any of the polypeptides described herein. For example, in some embodiments, the present invention relates to a nucleic acid sequence that encodes a polypeptide comprising,consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or any one or more of SEQ ID NOs: 1-14 or 50-244, 248-249, 257-349, or any one ormore of SEQ ID NOs: 1, 2, 15, 153, 304-349, or SEQ ID NO: 1 (and any of the above with a methionine at the N-terminus) or a fragment, homolog, or analog thereof. For example, the present invention provides for a polynucleotide sequence comprising, consisting essentially of, or consisting of the following sequence: [SEQ ID NO: 251: ttt ctg ccc tca]; [SEQ ID NO: 252: ttt ctg ccc tca gaa ttt gga gta gac gtagac aga] or other nucleic acid sequence that encodes a peptide of the invention including all nucleic acid sequences permitted under codon degeneracy which is the divergence in the genetic code which permits variation of nucleotide sequence withouteffecting the amino acid sequence of an encoded polypeptide. Accordingly, the instant invention relates to any nucleic acid sequence that encodes all or a substantial portion of the amino acid sequences set forth herein. Preferably any of the nucleotide sequences herein are preferably isolated and/or purified. The present invention also includes recombinant constructs comprising one or more of the nucleotide sequences described herein. Such constructs comprise a vector, such as a plasmid or viral vector, into which a nucleic acid sequence of theinvention has been inserted, in a forward or reverse orientation. In a preferred aspect of this embodiment, the construct further comprises regulatory sequences, including, for example, a promoter, operably linked to the sequence. Large numbers ofsuitable vectors and promoters are known to those of skill in the art, and are commercially available. Appropriate cloning and expression vectors for use with prokaryotic and eukaryotic hosts are also described in Sambrook et al. (2001, MolecularCloning: A Laboratory Manual, Cold Spring Harbor Press). Examples of such expression vectors include chromosomal, nonchromosomal and synthetic DNA sequences, e.g., derivatives of or Simian virus 40 (SV40); bacterial plasmids; phage DNA; baculovirus; yeast plasmids; vectors derived from combinations ofplasmids and phage DNA, viral DNA such as vaccinia, adenovirus, fowl pox virus, and pseudorabies. However, any other vector may be used as long as it is replicable and viable in the host. The appropriate nucleic acid sequence may be inserted into thevector by a variety of procedures. In general, a nucleic acid sequence encoding one of the polypeptides herein is inserted into an appropriate restriction endonuclease site(s) by procedures known in the art. Such procedures and related sub-cloningprocedures are deemed to be within the scope of those skilled in the art. The nucleic acid sequence in the expression vector is preferably operatively linked to an appropriate transcription control sequence (promoter) to direct mRNA synthesis. Examples of such promoters include: the retroviral long terminal (LTR) orSV40 promoter, the E. coli lac or trp promoter, the phage lambda PL promoter, and other promoters known to control expression of genes in prokaryotic or eukaryotic cells or their viruses. The expression vector also contains a ribosome binding site fortranslation initiation, and a transcription terminator. The vector may also include appropriate sequences for amplifying expression. In addition, the expression vectors preferably contain one or more selectable marker genes to provide a phenotypictrait for selection of transformed host cells such as dihydrofolate reductase or neomycin resistance for eukaryotic cell cultures, or such as tetracycline or ampicillin resistance in E. coli. The vector containing the appropriate nucleic acid sequences as described above, as well as an appropriate promoter or control sequence, may be employed to transform an appropriate host to permit the host to express the peptides herein (e.g., SEQID NOs: 1-256 or SEQ ID NOs: 1-24, 50-244, and 248-249, 257-305, or SEQ ID NOs: 1 or 2 or 153 or 304, or 305). Such vectors can be used in gene therapy. Examples of appropriate expression hosts include: bacterial cells, such as E. coli, Streptomyces, Salmonella typhimurium; fungal cells, such as yeast; insect cells such as Drosophila and Spodoptera frugiperda (Sf9); animal cells such as CHO, COS,HEK 293 or Bowes melanoma; adenoviruses; plant cells, etc. The selection of an appropriate host is deemed to be within the scope of those skilled in the art from the teachings herein. The invention is not limited by the host cells employed. Thus, in some embodiment, the present invention relates to methods for producing an analgesic peptide by transfecting a host cell (e.g., human cell or plant cell) with an expression vector comprising a nucleotide sequence that encodes a peptidecomprising, consisting essentially of, or consisting of an amino acid sequence of (or encoded by) any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or any of the above described polypeptides (e.g., any of theabove with a methionine at the N-terminal, or any analgesic fragment, or any antagonist, or any anti-pyretic thereof, or any homolog or analog thereof or multiple copies of any of the above polypeptides on a single vector). Such host cells are thencultured under a suitable condition, which allows for the expression of such peptides. The present invention further contemplates gene therapy using nucleic acids encoding one or more of the polypeptides herein (e.g., SEQ ID NOs: 1-349, or SEQ ID NOs: 1-24, 50-244, and 248-249, 257-349, or SEQ ID NOs: 1, 2, 153 or 304-349) or ananalog or homolog thereof. Preferably, such gene therapy is targeted. Targeted gene therapy involves the use of vectors (organ- and tumor-homing peptides) that are targeted to specific organs or tissues after systemic administration. The vectorconsisted of a covalent conjugate of avidin and a monoclonal antibody to a receptor. For example, for delivery to the brain, a chimeric peptide had been monobiotinylated, to a drug transport vector. The vector consisted of a covalent conjugate ofavidin and the OX26 monoclonal antibody to the transferrin receptor. Owing to the high concentration of transfernin receptors on brain capillary OX26 targets brain and undergoes receptor-mediated transcytosis through the blood-brain barrier (Bickel etal., 1993, Proc. Nat. Acad. Sci. 90:2618-2622). Another example is vector-mediated delivery of opioid peptides to the brain (NIDA Res Monogr. 1995, 154:28-46). In some embodiments, such nucleic acids are used to create a transgenic plant or animal, wherein the transgenic plant or animal is transgenic for a polynucleotide of the present invention and expresses a polypeptide of the present invention. Forintroducing a nucleic acid encoding one or more of the peptides herein into a plant cell, introduction can be carried out by conventional gene engineering techniques, for example, Agrobacterium infection, electroporation into protoplasts, particle gunmethods, and the like. In some embodiments, the nucleic acids above are introduced along with a second nucleic acid sequence or gene. In some embodiments, the second nucleic acid sequence can act as a promoter, etc. Preferably, the nucleic acid that is introduced into a plant cell is integrated into a vector having a selection marker gene. For example, the nucleic acids encoding any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-24,50-244, 248-249, or 257-349, or any one or more of SEQ ID NOs: 1, 2, 153, or 304-349, or a homolog or analog thereof can be integrated into one of such vectors (e.g., pGEM.RTM.-T and pBIN binary vectors). The vectors are then introduced into achromosome of a plant cell by homologous recombination (Fraley et al., 1983, Proc. Natl. Acad. Sci. USA, 80; 4803). Plant cells expressing the nucleic acids can then be selected. Alternatively, the nucleic acids can be introduced into a plant cellin a vector that is operably linked to a promoter and optionally a terminator both of which can function in the plant cell. Non-limiting examples of promoters that can function in a plant cell include constitutive promoters derived from T-DNA such as nopaline synthase gene promoter, octopine synthase gene promoter, etc., promoters derived from plant viruses such as19S and 35S promoters derived from cauliflower mosaic virus, etc., inductive promoters such as phenylalanine ammonia-lyase gene promoter, chalcone synthase gene promoter, pathogenesis-related polypeptide gene promoter, etc., and the like. Non-limiting examples of terminators that can function in a plant cell include terminators derived from T-DNA such as nopaline synthase terminator, terminators derived from plant viruses such as terminators derived from garlic viruses GV1, GV2,and the like. Plant cells into which such nucleic acids are introduced include plant tissues, whole plants, cultured cells, seeds and the like. Examples of the plant species into which the genes are introduced include dicotyledones such as tobacco, cotton,rapeseed, sugar beet, Arabidopsis thaliana, canola, flax, sunflower, potato, alfalfa, lettuce, banana, soybean, pea, legume, pine, poplar, apple, grape, citrus fruits, nuts, etc.; and monocotyledones such as corn, rice, wheat, barley, rye, oat, sorghum,sugar cane, lawn, etc. The second gene may also be introduced into such plant cells. The transformant plant cells expressing one or more of the polypeptides herein or homologs thereof can be obtained by culturing cells into which the gene is transferred in a selection culture medium corresponding to a selection marker joined tothe locus on the gene, for example, a culture medium containing a cell growth inhibitor, or the like, and isolating a clone capable of growing in the culture medium. Further, the selection culture medium should also correspond to a selection markerjoined to the locus of the second gene when the altered form of enzymatic activity is also present in the transformant plant cells. Alternatively, the above transformant plant cells can be selected by culturing plant cells into which the gene isintroduced in a culture medium containing the weed control compound to which the resistance is given, and isolating clones capable of growing in the culture medium. The plant expressing the desired peptide can be obtained from the transformant cells thus obtained by regenerating the whole plant according to a conventional plant cell culture method, for example, that described in Plant Gene ManipulationManual, Method for Producing Transgenic Plants, 1996, UCHIMIYA, Kodansha Scientific). Thus, the transformed plants such as plant tissues, whole plants, cultured cells, seeds and the like can be obtained. For example, rice and Arabidopsis thaliana expressing a gene encoding a desired peptide having the characteristics of having (i) anti-pyrogenic, (ii) anti-inflammatory, (iii) anti-neoplastic activity, or (iv) expressing resistance againstpathogen, or (v) expressing developmental changes such as an increase in the number of flowers (e.g., any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-24, 50-244, and 248-249, 257-349, or any one or more of SEQ ID NOs: 1-2, 153,or 304-349, or a homolog or analog thereof) can be obtained according to the method described in Experimental Protocol of Model Plants, Rice and Mouse-Ear Cress Edition, Chapter 4 (1996, Supervisors: Shimamoto and Okada, Shujun-sha), Further, accordingto the method, soybean expressing a gene encoding a desired peptide by introducing the gene into soybean adventitious embryo with a particle gun. Likewise, according to the method described by Fromm et al., 1990, Bio/Technol., 8:838, corn expressing thegene can be obtained by introducing the gene into adventitious embryo with a particle gun. Wheat expressing the gene by introducing the gene into sterile-cultured wheat immature scutellum with a particle gun according to a conventional method describedby Takumi, 1995, J. Breeding Soc., 44: Extra, 1:57. Likewise, according to a conventional method described by Hagio et al., 1995, J. Breeding Soc., 44; Extra, 1:67, barley expressing the gene encoding the above polypeptide can be obtained by introducingthe gene into sterile-cultured barley immature scutellum with a particle gun. Another embodiment is directed to fragments of the correspondent nucleic acid sequences, or the complement thereof, which may find use as, for example, hybridization probes or as antisense oligonucleotides. Such nucleic acid fragments areusually at least about 10 nucleotides in length, or at least about 20 nucleotides in length, or at least about 30 nucleotides in length, at least about 40 nucleotides in length, yet at least about 50 nucleotides in length, yet more, wherein in thiscontext the term "about" means the referenced nucleotide sequence length plus or minus 10% of that referenced length. In some embodiments, the present invention relates to methods for isolating a gene or gene fragment encoding a peptide of the invention (any one or more of SEQ ID NOs: 1-349 or a homolog or analog thereof) and homologs or analogs thereof fromvarious organisms. Such gene or gene fragment can have (i) anti-pyrogenic, (ii) anti-inflammatory, (iii) anti-neoplastic activity, or (iv) express resistance against pathogen, or (v) express developmental changes such as an increase in the number offlowers. Such gene or gene fragment can be identified by performing PCR using genomic DNA or cDNA of an organism having the desired gene as a template and primers produced on the basis of nucleotide sequences corresponding to those about the N- andC-termini of the polypeptide to amplify the desired gene. Further, genes encoding a peptide can be obtained from different organisms (e.g., a clone, a plant an animal, etc.). For example, first, a cDNA library is constructed by obtaining mRNA from anorganism and synthesizing cDNA by using the mRNA as template with reverse transcriptase and integrating the cDNA into a phage vector such as ZAP II, etc. or a plasmid vector such as pUC, etc. The cDNA library may be introduced into Escherichia colifollowed by subjecting a complementation test to select clones containing the desired gene derived from the desired organism. Further, for amplifying a DNA fragment containing at least a part of the desired gene, PCR can be carried out by using theabove-constructed cDNA library as a template and primers designed and synthesized on the basis of nucleotide sequences of the peptide. Screening of the cDNA library can be carried out by using the DNA fragment thus obtained as a probe to select positiveclones. The desired gene, i.e., a gene encoding a peptide substantially having at least one characteristics of (i) to, (v), can be confirmed by determination of the nucleotide sequence of the selected clone. 3. Antibodies In another embodiment, the invention provides for antibodies that specifically bind to any of the polypeptides herein. For example, the present invention contemplates an antibody that specifically binds to a peptide of having an amino acidsequence comprising, consisting essentially of, or consisting of any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, and 257-349, or any one or more of SEQ ID NOs: 1-14, 50-244, and 257-349, or any one or more of SEQ IDNOs: 1-2, 153, 304-349 or SEQ ID NO: 1, or any of the above with a methionine at the N-terminus, or any fragment, homolog, or analog thereof. The term "antibodies" is meant to include polyclonal antibodies, monoclonal antibodies, fragments thereof suchas F(ab')2, and Fab fragments, as well as any recombinantly produced binding-partners. Antibody can be prepared by conventional methods, e.g. by immunization of a human or of an animal, such as, for example, mouse, rat, guinea pig, rabbit, horse, sheep, goat, chicken (see also Messerschmid, 1996, BIOforum, 11:500-502), andsubsequent isolation of the antiserum; or by establishing hybridoma cells and subsequent purification of the secreted antibodies; or by cloning and expression of the nucleotide sequences, or modified versions thereof, which encode the amino acidsequences which are responsible for the binding of the natural antibody to the antigen and/or hapten. Antibodies of the invention are in particular those antibodies which bind to a polypeptide comprising, consisting essentially of, or consisting of anyone or more of: SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-24, 50-244, 248-249, and 257-349, or any one or more of SEQ ID NOs: 1-24, 50-163, 248-249, and 257-349, or any one or more of SEQ ID NOs: 1-2, 153, 304-349 or SEQ ID NO: 1. In someembodiments, such polypeptide has less than 100 amino acid residues, 90, 80, 70, 60, 50, 40, 30, 20, 10, 9, 8, 7, 6, 5, or 4 amino acid residues. In some embodiments, such polypeptide has between 4-100, 4-50, 440, 4-30, or 4-20 amino acid residues. Insome cases, such antibody selectively binds to the amino acid sequence Phe-Leu-Pro-Ser-Glu-Phe-Gly-Val-Asp-Val-Asp-Arg (SEQ ID NO: 2) or amino acid sequence Phe-Leu-Pro-Ser (SEQ ID NO: 1) The antibodies herein can specifically bind with a Ka of greater than or equal to about 104 M-1, or about 105 M-1, or about 106 M-1 or about 107 M-1. Affinities of binding-partners or antibodies canbe readily determined using conventional techniques, for example those described by Scatchard et al., 1949 (Ann. N.Y. Acad. Sci. 51:660) or, by surface plasmon resonance described by Wolff et al., 1993 (Cancer Res. 53:2560; BIAcore/Biosensor,Piscataway, N.J.), which are incorporated herein by reference for all purposes. Polyclonal antibodies can be readily generated from a variety of sources, for example, horses, cows, goats, sheep, dogs, chickens, rabbits, mice or rats, using procedures that are well known in the art. In general, an isolated polypeptide of theinvention (e.g., a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence of (or encoded by) any one or more of SEQ ID NOs: 1-349 or any of the above with an N-terminal methionine) that is appropriately conjugated, isadministered to the host animal typically through parenteral injection. The immunogenicity of the polypeptide may be enhanced through the use of an adjuvant, for example, Freund's complete or incomplete adjuvant. Following booster immunizations, smallsamples of serum are collected and tested for reactivity to the polypeptide. Examples of various assays useful for such determination include those described in Antibodies: A Laboratory Manual, Harlow and Lane (eds.), Cold Spring Harbor LaboratoryPress, 1988; as well as procedures such as countercurrent immuno-electrophoresis (CIEP), radioimmunoassay (RIA), radioimmunoprecipitation, enzyme-linked immunosorbent assays (ELISA), dot blot assays, and sandwich assays, see, e.g., U.S. Pat. Nos. 4,376,110 and 4,486,530, or other similar assays known in the art. Monoclonal antibodies specific for a desired polypeptide antigen (such as the peptides described herein) may be readily prepared using well-known procedures, see for example, the procedures described in Current Protocols in Immunolog (Wiley &Sons, NY, Coligan et al., eds., 1994; U.S. Pat. Nos. RE 32,011, 4,902,614, 4,543,439 and 4,411,993; Monoclonal Antibodies, Hybridomas: A New Dimension in Biological Analyses, 1980, Plenum Press, Kennett et al., eds.). Briefly, the host animals, suchas mice are injected intraperitoneally at least once, or at least twice at about three-week intervals with isolated and purified polypeptide herein (e.g., a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence of (orencoded by) any one or more of SEQ ID NOs: 1-349, or, conjugated polypeptide herein, optionally in the presence of adjuvant. Mouse sera are then assayed by conventional dot blot technique or antibody capture (ABC) to determine which animal is mostsuitable as a source of splenocytes for fusion to a myeloma partner cell-line. Approximately 2-3 weeks later, the mice are given an intravenous boost of the polypeptide. Mice are later sacrificed and spleen cells fused with commercially availablemyeloma cells, such as Ag8.653 (ATCC), following established protocols. Briefly, the myeloma cells are washed several times in media and fused to mouse spleen cells at a ratio of about three spleen cells to one myeloma cell. The fusing agent can be anysuitable agent used in the art, for example, PEG. The cell suspension containing fused cells is plated out into plates containing media that allows for the selective growth of the fused cells. The fused cells can then be allowed to grow forapproximately eight days. Supernatants from resultant hybridomas are collected and added to a plate that is first coated with goat anti-mouse Ig. Following washes, a label, such as, 125I-conjugated polypeptide (e.g., a polypeptide comprising,consisting essentially of, or consisting an amino acid sequence of (or encoded by) any one or more of SEQ ID NOs: 1-349, or any of the above with an N-terminal methionine) is added to each well followed by incubation. Positive wells can be subsequentlydetected by autoradiography. Positive clones can be grown in bulk culture and supernatants are subsequently purified over a Polypeptide A column (Pharmacia). The monoclonal antibodies of the invention can be produced using alternative techniques, such as those described by Alting-Mees et al., 1990 (Monoclonal Antibody Expression Libraries: A Rapid Alternative to Hybridomas, Strategies, Mol. Biol. 3:1-2469). Similarly, binding partners can be constructed using recombinant DNA techniques to incorporate the variable regions of a gene that encodes a specific binding antibody. Larrick et al. describe such technique in Biotechnol, 7:394, 1989. Other types of antibodies may be produced using the information provided herein in conjunction with the state of knowledge in the art. For example, antibodies that have been engineered to contain elements of human antibodies that are capable ofspecifically binding any of the peptide or to a polypeptide containing the peptide sequence herein are also encompassed by the invention. An additional method for selecting antibodies that specifically bind to a polypeptide, peptide or fragment thereofis by phage display, e.g., Winter et al., 1994, Annu. Rev. Immunol. 12: 433; Burton et al., 1994, Adv. Immunol. 57:191. Human or murine immunoglobulin variable region gene combinatorial libraries may be created in phage vectors that can be screenedto select Ig fragments (Fab, Fv, sFv, or multimers thereof) that bind specifically to a polypeptide, peptide, or fragment thereof. See, e.g., U.S. Pat. No. 5,223,409; Huse et al., 1989, Science: 1275; Kang et al., 1991 Proc. Natl. Acad. Sci. USA88:4363; Hoogenboom et al., 1992, J. Molec. Biol. 227:381; Schlebusch et al., 1997, Hybridoma 16:47, and references cited therein. For example, a library containing a plurality of polynucleotide sequences encoding Ig variable region fragments may beinserted into the genome of a filamentous bacteriophage, such as M13 or a variant or analog thereof, in frame with the sequence encoding a phage coat polypeptide, for instance, gene III or gene VIII of M13, to create an M13 fusion polypeptide. A fusionpolypeptide may be a fusion of the coat polypeptide with the light chain variable region domain and/or with the heavy chain variable region domain. Once isolated and purified, the antibodies may be used to detect the presence of a polypeptide, or apeptide of the present invention in a sample using established assay protocols. Further, the antibodies of the invention may be used therapeutically to bind to the peptides of the invention and alter their activity in vivo. Formulations Any of the composition herein may be formulated into pharmaceutical, veterinary, cosmetic and/or agricultural formulations for administration to an organism. Typically such formulations will include one or more acceptable carriers, excipients, or diluents. Pharmaceutically acceptable carriers for therapeutic use are well known in the pharmaceutical art, and are described, e.g., in Remington'sPharmaceutical Sciences, Gennaro, A R, ed., 20th edition, 2000: Williams and Wilkins Pa., USA. which is incorporate herein by reference for all purposes. Agriculturally acceptable carriers for therapeutic or prophylactic treatment of plants are alsoknown in the art. Cosmetic and veterinary excipients are also known in the art. For example, the compositions herein may be combined with one or more natural or synthetic, organic or inorganic material to facilitate their application into the plant. Such a carrier will generally be inert and acceptable in agriculture. Suchcarrier can be solid (e.g., clays, natural or synthetic silicates, silica, resins, waxes, or solid fertilizers) or liquid (e.g., water, alcohols, ketones, petroleum fractions, aromatic or paraffinic hydrocarbons, chlorinated hydrocarbons, or liquefiedgases). A pharmaceutical or agricultural formulation can also contain any kind of other compatible ingredients such as, for example, protective colloids, adhesives, thickening agents, thixotropic agents, penetrating agents, stabilizing agents,sequestering agents, fertilizers, anti-freeze agents, repellents, color additives, corrosion inhibitors, water-repelling agents, UV-stabilizers, pigments, dyes or polymers. In some embodiments, the compositions herein may be formulated as a salt and be formed with many acids, including but not limited to, hydrochloric, sulfuric, acetic, lactic, tartaric, malic, succinic, etc. Salts tend to be more soluble in aqueousor other protonic solvents than are the corresponding free base forms. In other cases, the preferred preparation may be a lyophilized powder which may contain any or all of the following: 1-50 mM histidine, 0.1%-2% sucrose, and 2-7% mannitol, at a pHrange of 4.5 to 5.5 that is combined with buffer prior to use. After pharmaceutically and physiologically acceptable compositions have been prepared, they can be placed in an appropriate container and labeled for treatment of an indicated condition. While any suitable carrier known may be employed in a pharmaceutical formulation of this invention, the type of carrier will vary depending on the mode of administration and whether a sustained release is desired. Routes of delivery may includeoral, inhaled, buccal, intranasal, and transdermal routes, as well as novel delivery systems such as the protective liposomes for oral delivery of peptides. For agricultural uses, formulations can be in a liquid or spray or any other dry formulations. For parenteral administration, such as subcutaneous injection, the carrier can include, e.g., any one or more of the following ingredients: water, saline, alcohol, a fat, a wax or a buffer. For oral administration, a carrier can comprise of carbohydrate or polypeptide fillers, such as sugars, including lactose, sucrose, mannitol, or sorbitol; starch from corn, wheat, rice, potato, or other plants; cellulose, such as methylcellulose, hydroxypropylmethyl-cellulose, or sodium carboxymethylcellulose; gums including arabic and tragacant; and polypeptides such as gelatin and collagen. If desired, disintegrating or solubilizing agents may be added, such as the cross-linkedpolyvinyl pyrrolidone, agar, alginic acid, or a salt thereof, such as sodium alginate. If desirable, the drug can be delivered in nanocapsules that would protect against proteolysis by proteases. Such carriers enable the compositions herein to beformulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for ingestion by the patient Pharmaceutical preparations for oral use can be obtained through a combination of active compounds with solidexcipient, suiting mixture is optionally grinding, and processing the mixture of granules, after adding suitable auxiliaries, if desired, to obtain tablets or dragee cores. As the composition may be peptide, such peptides can be put into a liposomalformulation to avoid degradation. The pharmaceutical formulations herein are administration by intravenous injection or by local applications (e.g., topical or subdermal). Formulations for topical administration can use a carrier that is a solution, emulsion, and ointment or gel base. The base, for example, may comprise one or more of the following: petrolatum, lanolin, PEGs, beeswax, mineral oil, diluents such aswater and alcohol, and emulsifiers and stabilizers. Thickening agents may be present in a pharmaceutical composition for topical administration. If intended for transdermal administration, the composition may include a transdermal patch oriontophoresis device. Biodegradable microspheres (e.g. polylactic galactide) may also be employed as carriers for the pharmaceutical compositions of this invention. Suitable biodegradable microspheres are disclosed, for example, in U.S. Pat. Nos. 4,897,268 and5,075,109. In this regard, it is preferable that the microsphere be larger than approximately 25 μm. Pharmaceutical compositions may also contain diluents such as buffers, antioxidants such as ascorbic acid, low molecular weight (less than about 10 residues) polypeptides, polypeptides, amino acids, carbohydrates including glucose, sucrose ordextrins, chelating agents such as EDTA, glutathione and other stabilizers and excipients. Neutral buffered saline or saline mixed with nonspecific serum albumin are exemplary appropriate diluents. In some cases the compositions herein are formulatedas a lyophilizate using appropriate excipient solutions (e.g., sucrose) as diluents. Pharmaceutically acceptable formulations include compositions wherein the active ingredients (e.g., a polypeptide comprising of, consisting essentially of, or consisting of an amino acid sequence of (or encoded by) any one or more of SEQ ID NOs:1-349, or any analog, or homolog thereof) are contained in an effective dose to achieve the intended purpose. The determination of an effective amount or dosage is well within the capability of those skilled in the art. Typically, an effective dose ofa polypeptide of the present invention (e.g., a polypeptide comprising of, consisting essentially of, or consisting of an amino acid sequence of (or encoded by) any one or more of SEQ ID NOs: 1-349, or any analog or homolog thereof) for systemicadministration is between about 0.001 μg to about 100 g, or between about 0.01 μg to about 50 g, or between about 0.1 μg to about 1 g, or between about 1 mg to about 500 mg per dose. For topical administration, the compositions herein may bedelivered at dosage up to about 99, 95, 90, 80, 70, 60, 50, 40, or 30% w/w of the composition. In some embodiments, the therapeutic effective dosages of SEQ ID NOs: 1-349 are the serum concentrations that in the range of 1-1000 mg/L, 5-500 mg/L, or 10-100 mg/L, or 10-20 mg/L or the active ingredient. Any of the compositions herein may be co-formulated or co-administered with a second therapeutic agent. Examples of therapeutic agents include, but are not limited to, analgesic, antipyretic medicaments (fever reducers), anesthetics,anti-rheumatic agents, anti-inflammatory agents, antidepressants, anti-neoplastic agents, antimicrobial agents (e.g., antibiotics, antiviral agents, and antifungal agents), pesticides, herbicides, angiogenic agents, anti-angiogenic agents, inhibitors ofneurotransmitters or neurotransmitters, any agent known to treat neurodegenerative conditions and wound healing, and combinations thereof. The concentration of an active ingredient in the composition of the present invention, as applied to plants can be within the range of 0.01 to 30.0% by weight, especially 0.1 to 30% by weight. In a primary composition, the amount of activeingredient can vary widely and can be, for example, from 5 to 95% by weight of the composition. For any of the compositions herein, the therapeutically effective dose can be estimated initially either in cell culture assays, e.g., of neoplastic cells, or in animal models, usually mice, rabbits, dogs, or pigs. The animal model may also beused to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans. Those of ordinary skill in the art are well able to extrapolate fromone model (be it an in vitro or an in vivo model). A therapeutically effective dose refers to that amount of active ingredient, for example a polypeptide comprising of, consisting essentially of, or consisting of an amino acid sequence of (or encodedby) any one or more of SEQ ID NOs: 1-349 or any fragment, analog, or homolog thereof, which ameliorates the symptoms or condition. Therapeutic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or experimentalanimals, e.g., ED50 (the dose therapeutically effective in 50% of the population) and LD50 (the dose lethal to 50% of the population). The dose ratio between therapeutic and toxic effects is the therapeutic index, and it can be expressed asthe ratio, LD50/ED50. Pharmaceutically and physiologically acceptable compositions, which exhibit large therapeutic indices, are preferred. The data obtained from cell culture assays and animal studies are used in formulating a range ofdosage for human use. The dosage contained in such compositions can be within a range of circulating concentrations that include the ED50 with little or no toxicity. The dosage varies within this range depending upon the dosage form employed,sensitivity of the patient, and the route of administration. The practitioner, in light of factors related to the subject that requires treatment, will determine the exact dosage. Dosage and administration are adjusted to provide sufficient levels ofthe active moiety or to maintain the desired effect. Factors, which may be taken into account, include the severity of the disease state, general health of the subject, age, weight, and gender of the subject, diet, time and frequency of administration,drug combination(s), reaction sensitivities, and tolerance/response to therapy. Long-acting pharmaceutically and physiologically acceptable compositions maybe administered every 3 to 4 days, every week, or once every two weeks depending on half-life andclearance rate of the particular formulation. Normal dosage amounts may vary from 0.001 μg to 100 g, up to a total dose of about 1 g, depending upon the route of administration. Guidance as to particular dosages and methods of delivery is provided in the literature and generallyavailable to practitioners in the art. Those skilled in the art will employ different formulations for nucleotides than for polypeptides or their inhibitors. Similarly, delivery of polynucleotides or polypeptides will be specific to particular cells,cell types, organism being treated, conditions, locations, etc. For example, for the prevention or treatment of pain, the appropriate dosage of an anti-pain medicament will depend on the type of condition to be treated, as defined above, the severity and course of the disease, whether the agent isadministered for preventive or therapeutic purposes or, as a combination with other drugs, previous therapy, the patients clinical history and response to the agent, and the discretion of the attending physician. The agent is suitably administered tothe patient at one time or over a series of treatments. Animal experiments provide reliable guidance for the determination of effective doses for human therapy. Interspecies scaling of effective doses can be performed following the principles laid down by Mordenti, J. and Chappell, W. "The use ofinterspecies scaling in toxicokinetics" in Toxicokinetics and New Drug Development, Yacobi et al., eds., Pergamon Press, New York 1989, pp. 42-96. For example, depending on the type and severity of the disease, about 0.001 μg/kg to 1000 mg/kg of atherapeteuric agent (peptide or small molecule described herein) is administered to a patient. For example, a daily dosage might range from about 0.1 mg/kg to 100 g/kg or more, depending on the factors mentioned above. In some cases, such as the administration of a composition comprising a peptide comprising Leu-Pro or Pro-Leu, an oraldose may be less than 100 mg/kg. Such dose can be repeated daily or at least 2, 3, 4, 5, 6, 7, 8, 9, or 10 times daily. Similar or greater dosages can be administered to a patient when a composition (pharmaceutical formulation) herein is administeredtopically. For example, a topical dose might range from 1 mg/m2 to 100 g/m2 and such dose can be applied topically daily or at least 2, 3, 4, 5, 6, 7, 8, 9, or times daily. The compositions herein can also be administered subdermally orsubcutaneously at appropriate ranges such as those described herein for example. For local administration or topical administration lower dosage may be required. For repeated administrations over several days or longer, depending on the condition, the treatment is sustained until a desired suppression of disease symptomsoccurs. However, other dosage regimens may be useful. The progress of this therapy is easily monitored by conventional techniques and assays. Guidance as to particular dosages and methods of delivery is provided in the literature; see, for example,U.S. Pat. Nos. 4,657,760; 5,206,344; or U.S. Pat. No. 5,225,212. It is anticipated that different formulations will be effective for different treatment compounds and different disorders, that administration targeting one organ or tissue, forexample, may necessitate delivery in a manner different from that to another organ or tissue. The compositions may be administered in the form of a solid, liquid, gel or gas (aerosol). For example, for oral administration, the composition pharmaceutical formulation) can be delivered as a syrup, lozenger, pill, gel capsule, etc. Forsubdermal or subcutaneous delivery, it can be delivered in a liquid formulation. For topical administration, the pharmaceutical composition can be delivered as a gel, cream or patch. The present invention contemplates a pharmaceutical formulation comprising: a peptide comprising dipeptide Leu-Pro or conservative substitution dipeptide thereof, or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite,or prodrug thereof or a nucleic acid encoding such peptide; and a pharmaceutical excipient. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising dipeptide Pro-Leu conservative substitution dipeptide thereof, or a homolog, derivative, or analog thereof, or a small molecule thereof, or asalt, metabolite, or prodrug thereof, or a nucleic acid encoding such peptide; and a pharmaceutical excipient. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising Xxx-Leu-Pro or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof, or a nucleic acid encodingsuch peptide; and a pharmaceutical excipient. In some cases, Xxx is an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution of any of the above, or ananalog or a derivative of any of the above. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising Xxx-Leu-Phe or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof, or a nucleic acid encodingsuch peptide; and a pharmaceutical excipient. In some cases, Xxx is an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution of any of the above, or ananalog or a derivative of any of the above. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising Leu-Pro-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof, or a nucleic acid encodingsuch peptide; and a pharmaceutical excipient. In some cases Xxx is an amino acid such as Tyr, Thr, Glu, Asp or Ser or a conservative substitution of any of the above, or an analog or a derivative of any of the above. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising Ser-Leu-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof, or a nucleic acid encodingsuch peptide; and a pharmaceutical excipient. In some cases, Xxx is an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution of any of the above, or ananalog or a derivative of any of the above. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising Xxx-Leu-Pro-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof, or a nucleic acidencoding such peptide; and a pharmaceutical excipient. In some cases, each of Xxx can be Tyr or Phe or Trp or His or Pro or an analog or a derivative thereof. In some cases, each of Xxx can be Phe or Ser or a conservative substitution of any of theabove, or an analog or a derivative of any of the above. The present invention also contemplates a pharmaceutical formulation comprising: a peptide comprising Xxx-Pro-Leu-Xxx or a homolog or analog thereof, or a small molecule thereof, or a salt, metabolite, or prodrug thereof, or a nucleic acidencoding such peptide; and a pharmaceutical excipient. In some cases, each of Xxx can be Tyr or Phe or Trp or His or Pro or an analog or a derivative thereof. In some cases, each of Xxx can be an aromatic amino acid or a derivative or analog thereof. For example, in some cases Xxx is Tyr or Phe or Trp or His or Pro or a conservative substitution of any of the above, or an analog or a derivative of any of the above. In some cases, Xxx is Ser or a conservative substitution of Ser, or an analog or aderivative of Ser. The present invention also specifically contemplates pharmaceutical formulation comprising a composition comprising, consisting, or consisting essentially of tripeptides such as: Phe-Leu-Pro (SEQ ID NO: 344), Trp-Leu-Prp, Tyr-Leu-Pro, Pro-leu-Phe(SEQ ID NO: 346), Pro-Leu-Trp, and Pro-Leu-Tyr. Any of the above amino acids can be substituted by a conservative substitution, or an analog or derivative of any of the above. The invention also contemplates non-linear (e.g., cyclic) forms of the aboveand small molecules equivalent to any of the above. Any of the excipients described herein or any other ones known in the art can be used according to the present invention. The pharmaceutical composition is formulated so as to allow the active ingredients contained therein to be bioavailable upon administration of the composition to a patient. Compositions that will be administered to a patient take the form of oneor more dosage units, where for example, a tablet may be a single dosage unit, and a container of one or more compounds of the invention in aerosol form may hold a plurality of dosage units. For oral administration, an excipient and/or binder may be present. Examples are sucrose, kaolin, glycerin, starch dextrins, sodium alginate, carboxymethylcellulose and ethyl cellulose. Coloring and/or flavoring agents may be present. Acoating shell may be employed. The composition may be in the form of a liquid, e.g., an elixir, syrup, solution, emulsion or suspension. The liquid may be for oral administration or for delivery by injection, as two examples. When intended for oral administration, preferredcompositions contain, in addition to the compositions herein one or more of a sweetening agent, preservatives, dye/colorant and flavor enhancer. In a composition intended to be administered by injection, one or more of a surfactant, preservative,wetting agent, dispersing agent, suspending agent, buffer, stabilizer and isotonic agent may be included. Injectable formulations of the compositions herein are preferably sterile. Means for achieving sterility are well known in the art. For delivery to the dermis and/or epithelium, dermal patches and delivery systems, utilizing active or passive transdermal delivery carriers may be prepared suing well known methods and materials, including, for example, microporous membranes,silicon polymers and diffusion matrixes. Such materials and methods are described, for example, in: Remington's Pharmaceutical Sciences, supra. For use in plants, the compositions of the invention are generally applied to seeds, plants or their habitat. Thus, the compositions herein can be applied directly to the soil before, at or after drilling so that the presence of active compoundin the soil can control the growth of pathogens, which may attack the seeds. When the soil is treated directly with a composition herein, it can be applied in any manner which allows it to be intimately mixed with the soil, e.g., by spraying, bybroadcasting a solid form of granules, or by applying the active ingredient at the same time as drilling by inserting it in the same drill as the seeds. A suitable application rate is within the range of from 0.005 to 1000 g per hectare, or from 0.10 to500 g per hectare. Alternatively, the active compounds can be applied directly to a plant by, for example, spraying or dusting either at the time when a pathogen has begun to appear on the plant or before the appearance of a pathogen as a protective measure. Inboth such cases the preferred mode of application is by foliar spraying. It is generally important to obtain good control of pathogens in the early stages of plant growth, as this is the time when the plant can be most severely damaged. The spray or dust can further contain a pre- or post-emergence herbicide if this is thought necessary. Sometimes, it is practicable to treat the roots, bulbs, tubers or other vegetative propagule of a plant before or during planting, forexample, by dipping the roots in a suitable liquid or solid composition. When the active compound is applied directly to the plant a suitable rate of application is from 0.002 to 5 kg per hectare, or from 0.005 to 1 kg per hectare, or from 0.01 to 0.05kg per hectare. Conditions Affecting Animals and Plants In some aspects, the present invention relates to uses of compositions such as the peptides disclosed herein (Table VI) for modulating, preventing, or treating condition(s) in an organism. Such organisms can be animals and/or plants. Examplesof animals include domesticated animals, such as dogs, cats, horses, cows, goats, sheep, chicken, and birds. Animals can also be humans. Plants can be crops such as wheat, barley, rice, corn, sugar, or soy; vegetables or fruits, such as apples, pears,citrus fruits, berries and nuts; and/or flowering plants such as roses, gardenias, orchids, carnations, bird of paradise, etc. But other plants or parts of plants are also contemplated herein (e.g., trees for lumber, such as fir, redwoods, pine, etc.) The conditions that are modulated, prevented, or treated by the compositions herein can be broadly classified as metabolic or mitochondrial conditions. More specifically, such conditions are e.g., thermogenic or pyrogenic conditions. Suchconditions can be associated with, for example, pain, temperature regulation, inflammation, neoplastic growth (e.g., cancer), innate immune response activation and ability to fight parasites and pathogens, skin and dermatological conditions, diabetesrelated disorders, wound healing, undesirable drug side effects, and neurological and neurodegenerative conditions. Such conditions can occur in a cell, group of cells, or an entire organism to be treated herein. 1. Pain In one aspect the present invention relates to treatment of pain. Examples of pain conditions contemplated by the invention include, but are not limited to, headaches (e.g., trigeminal neuralgia, sinusitis, cluster headaches, migraines, etc.),low back pain, cancer pain, arthritis pain, muscle spasm pain (muscle cramps), bone pain, pain resulting from burns, pain associated with bumps, pain associated with bruises, inflammatory pain (from an infection or arthritic disorder), pain fromobstructions, myofascial pain, pain from nerve trauma (dystrophy/causalgia), phantom limb pain, entrapment neuropathy (e.g., carpal tunnel syndrome), peripheral neuropathy, and pain from wounds, e.g., surgical, accidental, or self-inflicted wounds. The pathophysiology of pain can be broadly divided into three categories: (i) nociceptive pain, (ii) neuropathic pain, and (iii) idiopathic pain. (Willis, W. D., 1985, The Pain System. The Neural Basis of Nociceptive Transmission in theMammalian Nervous System. Pain and Headache, vol. 8, Gildenberg P L (Ed.) Karger Publishers, New York). Nociceptive pain is the result of receptor stimulation by tissue injury. It involves the normal activation of the nociceptive system by noxious stimuli. Examples of nociceptive pain include sprains, bone fractures, burns, bumps, bruises,inflammation (from an infection or arthritic disorder), obstructions, myofascial pain (which may indicate abnormal muscle stresses) headaches, low back pain, cancer pain, and arthritis pain. In some embodiments, the compositions herein are used toprevent or treat nociceptive pain. Such compositions include, e.g., those that comprise a peptide comprising any one or more of SEQ ID NOs: 1-349, or SEQ ID NO: 1-244, 248-249, and 257-349 or: SEQ ID NOs: 1, 2, 153, 304-349, or SEQ ID NO: 1. Suchcomposition can comprise a nucleic acid encoding an amino acid sequence of any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-244, 248-249, and 257-349 or any one or more of: 1, 2, 153, or 304-349. Such compositions can alsoinclude a small molecule that mimics a peptide comprising any one or more of: SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-244, 248-249, and 257-349 or any one or more of: SEQ ID NOs: 1, 2, 153, 304-349, or SEQ ID NO: 1. In some embodiments,second therapeutic agent(s) such as NSAIDs (on-Steroidal Anti-Inflammatory Drugs), and/or opioids, and/or antagonists can be used in combination with the compositions herein to treat nociceptive pain. Thus, in one aspect, the present invention relates to uses of the compounds herein for treating nociceptive pain. Such methods involve administering one or more of the compositions herein to a subject suffering or susceptible of sufferingnocicpetive pain. Such composition can include, e.g., a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence of any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-14, 50-152, 248-249, and257-349, or any one or more of SEQ ID NOs: 1-2, 153, 304-349 or SEQ ID NO: 1. In one embodiment, such composition comprises a nucleic acid sequence that encodes a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequenceof any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-14, 50-152, 248-249, and 257-349, or any one or more of SEQ ID NOs: 1-2, 153, 304-349 or SEQ ID NO: 1. In one embodiment, such composition comprises an antibody thatspecifically binds a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence of any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-14, 50-152, 248-249, and 257-349, or any one or more of SEQ IDNOs: 1-2, 153, 304-349 or SEQ ID NO: 1. In some embodiment, the composition comprises a small molecule that mimics a polypeptide of any one or more of SEQ ID NOs: 1-349, or any one or more of SEQ ID NOs: 1-14, 50-152, 248-249, and 257-349, or any one ormore of SEQ ID NOs: 1-2, 153, 304-349 or SEQ ID NO: 1. The second category of pain, neuropathic pain, is the result of an injury or malfunction in the peripheral or central nervous system. Examples of neuropathic pain include post herpetic (or post-shingles) neuralgia, reflex sympatheticdystrophy/causalgia (nerve trauma), components of cancer pain, phantom limb pain, entrapment neuropathy (e.g., carpal tunnel syndrome), and peripheral neuropathy most commonly caused by diabetes or chronic alcohol use. Neuropathic pain is often triggered by an injury, but this injury may or may not involve actual damage to the nervous system. For example, nerves can be infiltrated or compressed by tumors, strangulated by scar tissue, or inflamed by infection,which may cause neuropathic pain. Neuropathic pain may persist for months or years beyond the apparent healing of any damaged tissues. Therefore, neuropathic pain is frequently chronic, not fully reversible, and tends to have a less robust response totreatment with opioids, but may respond to drugs such as anticonvulsants (carbamazepine and valproic acid, and gabapentin) and neuromodulating drugs (including tricyclic antidepressants, such as amitriptyline, imipramine, and desipramine). The present invention contemplates uses of the compositions herein for treatment of neuropathic pain. In particular, the present invention includes methods for treating neuropathic pain in a subject by administering one or more of thecompositions herein to the subject in a therapeutically effective amount to treat or prevent neuropathic pain. In preferred embodiment, the composition herein used to treat neuropathic pain comprises or consists essentially or consists of a polypeptidecomprising, consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349, or an analog, salt, polymorph, metabolite, or prodrug thereof. In one embodiment, such composition comprises a nucleic acidsequence that encodes a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349, or a homolog or an analog thereof. In one embodiment, such composition comprises an antibodythat specifically binds a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349 or an analog or homolog thereof. The third category of pain, idiopathic pain, is a diagnosis of exclusion in which a patient suffers pain for longer than 6 months for which there is no physical cause and no specific mental disorder. Examples of idiopathic pain include, but arenot limited to, arthritis, fibromyalgia, chronic fatigue syndrome, irritable bowel syndrome, interstitial cystitis, vulvadynia, carpal tunnel syndrome, etc. In one aspect, the present invention relates to uses of the compounds herein for treating idiopathic pain. Such methods involve administering one or more of the compositions herein to a subject suffering or susceptible of suffering idiopathicpain. Such composition preferably include a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349, or an analog, salt, polymorph, metabolite, or prodrug thereof. In oneembodiment, such composition comprises a nucleic acid sequence that encodes a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349, or a homolog or an analog thereof. Inone embodiment, such composition comprises an antibody that specifically binds a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence such as any one or more of SEQ ID NOs: 1-349 or an analog or homolog thereof. Any of the compositions herein can be administered either singly or in combination with a second therapeutic agent such as an analgesic pain reliever or anti-inflammatory. In some embodiments, the second therapeutic agent is co-formulated withone or more of the compositions (e.g., polypeptides or analogs, i.e., small molecules equivalent thereof) herein. According to the National Drag Classification (NDC), analgesics can be categorized into the following group: general analgesic, narcotic analgesic, non-narcotic analgesic, anti-arthritics, anti-migraine/headache, central pain syndrome, NSAID,anti-pyretic, and anti-menstrual pain products. These categories can be combined into broader categories of analgesics entitled: narcotic analgesics, non-narcotic analgesics, and NSAIDs. The present invention relates to a pharmaceutical formulation comprising the combination of the compositions herein (e.g., polypeptides, small molecules equivalent thereof, nucleic acids, antibodies) with one or more analgesic agents selectedfrom the group consisting of general analgesic, narcotic analgesic, non-narcotic analgesic, anti-arthritics, anti-migraine/headache, central pain syndrome, NSAID, anti-pyretic, and anti-menstrual pain products. The present invention also relates to apharmaceutical formulation comprising the combination of the polypeptides herein with one or more analgesics selected from the group consisting of narcotic analgesics, non-narcotic analgesics, and NSAIDs. The present invention also relates to methods oftreating a subject suffering from pain (e.g., nociceptive pain, neuropathic pain, and idiopathic pain) comprising administered to the subject the one or more compositions herein and the one or more analgesics described herein (either separately or incombination, as a co-formulation or in two separate formulations). Examples of narcotic analgesics include, but are not limited to, Alfentanil; Allylprodine; Alphaprodine; Amiphenazole, Anileridine, Benzoylhydrazone, Benzylmorphine, Benzitramide, Nor-Binaltorphimine, Bremazocine; Bupremorphine; Butorphanol(Stadol.RTM.); Clonitazene; Codeine; CTOP; Cyclazocinc; DAMGO; Desomorphine; Dextromoramide; Dezocine; Diampromide; Dihydrocodeine; Dihydrocodeine enol acetate; Dihydromorphine; Dimenoxadol; Dimepheptanol; Dimethylthiambutene; Dioxaphetyl Butyrate;Dipipanone; Diprenorphine; DPDPE; Eptazocine; Ethoheptazine; Ethylketocyclazocine; Ethylmethylthiambutene; Etonitazene; Etorphine; Fentanyl (Sublimaze.RTM., Duragesic.RTM.); Hydrocodone; Hydromorphone (Dilaudid.RTM.); Hydroxypethidine; Isomethadone;ketobemidone; Levorphanol; Levallorphan; Lofentanil; Loperamide; Meperidine (Demerol.RTM.); Meptazinol; Metazocaine; Methadone (Dolophine.RTM.); Metopon; Morphine (Roxanol™); Myrophine; Nalbuphine; Nalmefene; Nalorphine; Naloxone; Naltrindole;Naltrexone; Narceine; Nicomorphine, Norlevorphanol; Normethadone; Normorphine; Norpipanone; Opium; Oxycodone (OxyContin.RTM.); Oxymorphone; Papavereturn; Papaverine; Pentazocine; Phenadoxone; Phenazocine; Phenoperidine; Piminodine; Piminodine;Proheptazine; Promedol; Propiram; Propoxyphene (Darvon.RTM.); Remifentanil; Spiradoline; Sufentanil; Tilidine; U50,488; and U69,593. Some products are combination drugs; codeine/acetaminophen (APAP; Tylenol.RTM. #3); hydrocodone/acetaminophen(Vicodin.RTM.); Oxycodone/ASA (Percodan.RTM.); oxycodone/APAP (Percocet.RTM.); propoxyphene/ASA (Darvon Compound™); propoxyphene/napsylate (Darvocet-N.RTM.); hydrocodone/ibuprofen (Vicoprofen.RTM.); pentazocine/naloxone (Talwin-Nx.RTM.). Examples of non-narcotic analgesics, include, but are not limited to, Acetaminophen (Paracetamol; Tylenol.RTM.); aspirin (acetylsalicylic acid; Anacin.RTM., Ascriptin.RTM., Bayer.RTM., Bufferin.RTM., Ecotrin.RTM., Excedrin.RTM.); AminobenzoicAcid; Capsaicin (Zostrix.RTM. and Zostrix.RTM.-HP); Carbaspirin Calcium; Choline and Magnesium Salicylates (CMT.RTM., Tricosal.RTM., Trilisate.RTM.); Choline Salicylate (Arthropan.RTM.); Etanercept; Fluprednisolone; Gold sodium Thiomalate; Gold SodiumThiosulfate; Hyaluronic Acid; Homomethyl Salicylate; Leflunomide; Magnesium Salicylate (Arthritab.RTM., Bayer.RTM. Select, Doan's Pills.RTM., Magan.RTM., Mobidin.RTM., Mobigesic.RTM.); Menthol; Methorexate; Octyl Salicylate; Oxyphenbutazone; PhenylSalicylate; Phenylbutazone; Prednisolone; Salicylamide; Salsalate (Amigesic.RTM., Anaflex.RTM. 750, Disalcid.RTM., Marthritic.RTM.; Mono-Gesic.RTM., Safflex.RTM., Salsitab.RTM.); Sodium Hyaluronate; Sodium Salicylate; o-Acetylsalicyloyl Chloride; SodiumThiosalicylate (Thiocyl); Tramadol; Triamcinilone; Triethanolamine Salicylate (Trolamine); Zomepirac. Some products, such as Excedrin.RTM., are combination drugs (Excedrin.RTM. is acetaminophen, ASA, and caffeine). Other non-narcotic gabapentin(Neurontin.RTM.); lamotrigine and, anti-convulsants and tricyclic anti-depressants such as carbamazepine, pregabalin and duloxetine Examples of NSAIDS include, but are not limited to, Bromfenac Sodium; Celecoxib (Celebrex.RTM.); Diclofenac Potassium (Cataflam.RTM.); Diclofenac Sodium (Voltaren.RTM., Voltaren.RTM. XR); Diclofenac Sodium with misoprostol (Arthrotec.RTM.);Diflunisal (Dolobid.RTM.); Etodolac (Lodine.RTM., Lodine.RTM.XL); Etadolac; Fenoprofen calcium (Nalfon.RTM.); Flurbiprofen (Ansaid.RTM.); Ibuprofen (Motrin.RTM., Advil.RTM., Nuprin.RTM.); Indomethacin (Indocin.RTM., Indocin.RTM. SR); Ketoprofen(Actron.RTM., Orudis.RTM., Orudis KT.RTM., Oruvail.RTM.); Meclofenamate Sodium Meclomen.RTM.); Mefenamic acid (Ponstel.RTM.); Meloxicam (Mobic.RTM.); Nabumetone (Relafen.RTM.); Naproxen (Naprosyn.RTM., Naprelan.RTM., Aleve.RTM., Anaprox.RTM.); Oxaprozin(Daypro.RTM.); Piroxicam (Feldene.RTM.); Piroxicam (Feldene.RTM.); Rofecoxib (Vioxx.RTM.); Sulindac (Clinoril.RTM.); Suprofen; Tolmetin Sodium (Tolectin.RTM.); Valdecoxib (Bextra.RTM.). Examples of antagonists include, but are not limited to, Alvimopan, trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine; ANTI, 5'-acetamidinoethylnaltrindole; 4-Aminoquinoline; N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamidemonohydrochloride; Benzimidazolinone; 7-Benzylidenenaltrexone; Binaltorphimine; nor-Binaltorphimine; Butorphanol (17-cyclobutylmethyl-3,14-dihydroxymorphinan) tartrate; CTAP, D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2; CTOP,D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr-NH2 (SEQ ID NO: 32); Cyclazocine; Cyprodime; 1,3-Dimethyl-4-piperidinone; Ethylketocyclazocine; β-Funaltrexamine; GNTI, 5'-Guanidinonaltrindole; ICI 174864, N,N-diallyl-Tyr-Aib-Aib-Phe-Leu (SEQ ID NO: 40);Indolomorphinan; 5 -Isothiocyanate; J-113397, 1-[(3R,4R)-1-Cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-di- hydro-2H-benzimidazol-2-one; JDTic, (3R)-7-Hydroxy-N-[(1S)-1-[[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-pip-eridinyl]methyl]-2-methylpropyl]-1,2,3,4-tetrahydro-3-isoquinoline-carboxa- mide 3-Quadazocine; Loperamide; Methoxynaltrexone; Methylnaltrexone; Mr 2266; Nalmefene; Nalorphine; Naloxone; Naloxone methiodide; Naloxazone; Naltrexone; β-Naltrexamine;Naltriben; Naltrindole; Phenylpiperidine; SB-612111, (-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9- -tetrahydro-5H-benzocyclohepten-5-ol; SoRI 9409, 59-(4-chlorophenyl)-17-(cyclopropylmethyl)-6,7-didehydro-3,14-dihydroxy-4-,5a-epoxypyrido-[29, 39:6,7]morphinan, SNC 80; TIPP-y, Tyr-Tic-Phe-Phe; Triethyleneglycolnaltrexamine. Furthermore, there are various naturally occurring and synthetic opioids that can be used to treat pain. See Table II below. TABLE-US-00002 TABLE II List of opioid peptides Enkephalins [Leu]-enkephalin YGGFL (SEQ ID NO: 15) [Met]-enkephalin YGGFM (SEQ ID NO: 16) Rimorphin YGGFLRRQFKVVT (SEQ ID NO: 248) Leumorphin KYPKRSSEVAGEGDGDSMGHEDLYKRYGGFLRRIRPKLKWDNQKRYGGFLRRQFKVVTRSQEDPNAYSGELF DA (SEQ ID NO: 249) Endorphins α-Neoendorphin YGGFLRKYPK (SEQ ID NO: 17) β-Neoendorphin YGGPLRKYP (SEQ ID NO: 18) β-human-Endorphin YGGFMTSEKSQTPLVTLFKNAIIKNAYKKGE (SEQ ID NO: 19)α-human-Endorphin YGGFMTSEKSQTPLVT (SEQ ID NO: 20) Dynorphins DynorphinA YGGFLRRIRPKLKWDNQ (SEQ ID NO: 21) Dynorphin B YGGFLRRQFKVVT (SEQ ID NO: 22) Endomorphins Endomorphin-1 YPTF (SEQ ID NO: 23) Endomorphin-2 YPFF (SEQ ID NO: 24) Syntheticpeptides [D-Ala2, N-Me-Phe4, Gly5-ol]- [Tyr-D-Ala-Gly-N-Methyl-Phe-Gly-ol enkephalin (DAMGO; DAGO) (SEQ ID NO: 25) D-Pen2,5]-enkephalin (DPDPE) [Tyr-D-Pen-Gly-Phe-D-Pen (SEQ ID NO: 26) D-Pen2,5]-enkephalin Tyr-D-Pen-Gly-D-Chloro-Phe-D-Pen (pCl-DPDPE)(SEQ ID NO: 27) [D-Pen2, Pen5]-enkephalin Tyr-D-Pen-Gly-Pen-Pen (DPLPE) (SEQ ID NO: 28) [D-Ser2, D-Leu5]-enkephalin-Thr Tyr-D-Ser-Gly-Phe-Leu-Thr (DSLET) (SEQ ID NO: 29) [D-Ala2, D-Leu5]-enkephalin Tyr-D-Ala-Gly-Phe-D-Leu (DADLE) (SEQ ID NO: 30)Met-enkephalin-Arg-Phe (MERF) Tyr-Gly-Gly-Phe-Met-Arg-Phe (SEQ ID NO: 31) CTOP D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr (SEQ ID NO: 32) Ac-RYYRIK Ac-Arg-Tyr-Arg-Ile-Lys (SEQ ID NO: 33) ([D-Arg2, Lys4]-Dermorphin1)- Tyr-D-Arg-Phe-Lys amide (DALDA) (SEQ ID NO:34) (D-Ala2,N-Methyl-Phe4, Tyr-D-Ala-Gly-N-Methyl-Phe-Gly-ol Met(O)5-ol]-enkephalin (SEQ ID NO: 35) (FK-33824) [D-Ala2,Leu5,Cys6]-enkephalin Tyr-D-Ala-Gly-Phe-D-Leu-D-Cys (DALCE) (SEQ ID NO: 36) [D-Ala2 Glu4]-Deltorphin II Tyr-D-Ala-Phe-Glu-Val-Val-ProGly-amide (SEQ ID NO: 37) [D-Ala2]Deltorphin 1 Tyr-D-Ala-Phe-Asp-Val-Val-Gly (SEQ ID NO: 38) PL-O17 Tyr-Pro-Methyl-Phe-D-Pro (SEQ ID NO: 39) ICI 174,8674 N,N-diallyl-Tyr-Aib-Aib-Phe-Leu (SEQ ID NO: 40) Others Morphiceptin YPFP (SEQ ID NO: 41) Nociceptinorphanin FQ FGGFTGARKSARKLANQ (SEQ ID NO: 42) Nocistatin TEPGLEEVGEIEGQKQLQ (SEQ ID NO: 43) Neuropeptide AF human AGEGLNSQFWSLAAPQRF (NPAF) (SEQ ID NO: 44) Neuropeptide SF human SQAFLFQPQRF (NPSF) (SEQ ID NO: 45) Substrate P RPKPQQFFGLM (SEQ ID NO: 46)β-human-Casomorphin YPFVEPIP (SEQ ID NO: 47) β-bovine-Casomorphin YPFPGPI (SEQ ID NO: 48) Of the above opioids β-endorphins, enkephalins, and dynorphin are three human endogenous opioids. β-endorphins are primarily found in the arcuate nucleus of the hypothalamus and in the pituitary gland, a feature that distinguishes thisgroup from the enkephalins, which are not present in that area. Enkephalins may be broken down into two types, methionoine enkephalin (met-enkephalin) and leucine enkephalin (leu-enkephalin), and their ratio is 4:1 respectively. They are more widelydistributed in the brain than β-endorphins, being present in several areas including hypothalamic nuclei, limbic structures, caudate-putamen, the brain stem, several layers of the dorsal horn, peripheral nerves, and the adrenal medulla. The mostpowerful of the opioids, dynorphins, are found throughout the central and peripheral nervous systems. Some research supports the theory that they regulate pain at the spinal cord level, influence feeding behavior at the hypothalamic level, and functionwith other endogenous opioids to regulate the cardiovascular system. Dynorphins also may be involved in inhibiting intestinal motility, a phenomena that occurs when the body perceives pain. The presence of a large precursor to this opioid in theanterior pituitary suggests that it has many peripheral targets. Another opioid called neo-endorphin also is classified in the Dynorphin group. The endogenous opioid system has been used to treat chronic pain through a technique called neuroaugmentation that involves electrical stimulation of specific areas of the brain to increase the quantity and reactivity of endogenous opioids. Partial or complete pain relief has been noted in patients treated with neuroaugmentation; lower levels of efficacy were observed in severely ill cancer patients. Spinal cord stimulation was found to be successful in treating chronic pain not associatedwith malignancy. In some embodiments, the present invention contemplates the use of an opoid, e.g., any of the opioids herein (whether naturally occurring or not) to modulate heat production, or to modulate the innate immune mechanisms, or to modulatemitochondrial activity in plants and/or animals. It should be noted that for the treatment/prevention/alleviation of pain, the compositions described herein can be used as analgesics as well as anesthetics. 2. Temperature Regulation In one aspect, the compositions herein can also be used to regulate body temperature of an animal or a plant by modulating the outflow and inflow of heat from the body. Fever, an elevated core body temperature, is the most commonthermoregulatory change that often accompanies inflammation and/or infection. One main source of heat in both plants and animals is the mitochondria. Another major source of heat in animals is muscular contraction. However, in plants, it is oftendifficult to measure their body/appendix temperature because the amount of heat produced is relatively small and the there is a large amount of heat loss to the environment. In humans, opioids that have been used to alleviate pain have been linked to some degree with temperature regulation in humans. In particular, there is some evidence that suggests a link between the nervous system and thermoregulation(Thermoregulation, Tenth International Symposium on the Pharmacology of Thermoregulation. Blatteis C M, Ed., Annal. NY Acad. Sci. vol., 813, 1997), and more specifically between opioid peptides and thermoregulation (Adler M W et al, 1988, OpioidSystem and Temperature Regulation, Annu. Rev. Pharmacol. Toxicol., Vol. 28: 429-450). In one aspect, the present invention relates to the surprising discovery that analgesics, such as opioids useful in treating pain in humans, can also be used to modulate heat production in plants. Thus, the present invention relates to uses ofany of the compositions herein including for example (i) polypeptides comprising, consisting essentially of, or consisting of, any one or more of amino acid sequences SEQ ID NOs: 1-349 or any one or more of amino acids sequences SEQ ID NOs: 50-244,248-249, 257-349, or any one or more of amino acid sequences SEQ ID NOs: 1-14, 50-244, 257-349, or any one or more of amino acid sequences SEQ ID NOs: 1-2 or SEQ ID NO: 1 or an analog or homolog of any of the above; (ii) nucleic acids encoding any of theabove polypeptides; (iii) antibody or antibody fragment that specifically bind any of the above polypeptides, or small molecules or nucleic acids; and (iv) small molecules or analogs of the above polypeptides. Such heat production modulation can be used e.g., to prevent frost damage to the seed and plants. It can also increase the innate immune response of the plants (discussed in more detail below). The above uses can be accomplished byadministering to a plant or seed any of the above compositions with an agricultural excipient via spray, drip irrigation or other irrigation, dipping at least a portion of said plant or seed in said composition, coating at least partially said plant orseed with said composition, etc. In another embodiment, a nucleic acid sequence encoding any of the above compositions can be used to transfect plants such that their heat production is regulated. In another aspect, the present invention relates to methods of using the above compositions for modulating mitochondrial activity in plants and animals. Modulating mitochondrial activity can be used to prevent, treat, or ameliorate mitochondrialconditions in plants and animals. Examples of mitochondrial conditions include, but are not limited to, Alpers disease (progressive infantile poliodystrophy); Barth syndrome (cardiomyopathy-neutropenia syndrome); lethal infantile cardiomyopathy (LIC); Beta-oxidation defects;carnitine deficiency and disorders; chronic progressive external ophthalmoplegia syndrome (CPEO); Kearns-Sayre syndrome (KSS); lactic acidosis; Leber hereditary optic neuropathy (LHON); Leigh disease (subacute necrotizing encephalomyelopathy); long-chainacyl-CoA dehydrogenase deficiency (LCAD); Luft disease; medium-chain acyl-CoA dehydrogenase deficiency (MCAD); mitochondrial cytopathy; mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (MELAS); mitochondrial encephalopathy;mitochondrial myopathy; multiple acyl-CoA dehydrogenase deficiency (MAD); glutaric aciduria Type II; myoclonic epilepsy and ragged-red fiber disease (MERRF); myoneurogastrointestinal disorder and encephalopathy (MNGIE); neuropathy ataxia and retinitispigmentosa (NARP); Pearson syndrome; pyruvate carboxylase deficiency; pyruvate dehydrogenase deficiency (PHD); and short-chain acyl-CoA dehydrogenase deficiency (SCAD). Other examples of mitochondrial conditions include respiratory chain disorders such as: Complex I: NADH dehydrogenase (NADH-CoQ reductase) deficiency; Complex II: Succinate dehydrogenase deficiency; Complex III: ubiquinone-cytochrome coxidoreductase deficiency; Complex IV: cytochrome c oxidase (COX) deficiency; and Complex V: ATP synthase deficiency. In one embodiment, an organism such as a plant or animal can be diagnosed for the presence of a mitochondrial condition by genetically screening the organism. In some embodiments, the organism's genetic DNA or mitochondrial DNA can be analyzed. In some embodiments, the organism's RNA, mRNA, siRNA, or cRNA is analyzed. An organism having or susceptible of having a mitochondrial condition can then be administered one or more of the compositions disclosed herein to modulate, treat, or prevent the condition. Such compositions include, but are not limited to:polypeptides comprising, consisting essentially of, or consisting of, any one or more of amino acid sequences SEQ ID NOs: 1-349, or any one or more of amino acids sequences SEQ ID NOs: 50-244, 248-249, 257-349, or any one or more of amino acid sequencesSEQ ID NOs: 1-14, 50-244, 257-349, or any one or more of amino acid sequences SEQ ID NOs: 1-2 or SEQ ID NO: 1 or an analog or homolog of any of the above; (ii) nucleic acids encoding any of the above polypeptides; (iii) an antibody or antibody fragmentthat specifically binds a polypeptide comprising any one or more amino acid sequences: SEQ ID NOs: 1-304 or any one of amino acid sequences SEQ ID NOs: 1-14, 50-244, 257-349; and (iv) small molecules or analogs of the above polypeptides. 3. Inflammation Acute and chronic pain is frequently associated with inflammation as a result of tissue destruction, abnormal immune reactivity or nerve injury. In one aspect, the compositions herein can also be used to treat, modulate, or prevent inflammation in an organism. The inflammation can be due to a variety of external or internal insults, such as infectious agents, physical injury, hypoxia, ordisease processes in nearly any organ or tissue in the body with one or more of the following symptoms: redness, heat, tenderness/pain, and swelling. Other examples are inflammatory diseases which the compositions herein can be used to treat includethose such as rheumatoid arthritis, inflammatory bowel disease, scleroderma, cutaneous lupus erythematosus, systemic lupus erythematosus, type I and II diabetes, asthma, multiple sclerosis, abscess, wounds, meningitis, encephalitis, vasculitis, andcardiovascular diseases. Since the discovery of salicylic acid (SA) as an anti-inflammatory compound and the subsequent synthesis of aspirin (ASA) over a century ago, several classes of structurally diverse compounds have become available for the treatment of humaninflammatory disorders. These compounds are collectively known as NSAIDs and share with ASA a common mechanism by which they exert their anti-inflammatory action. Inflammation is now recognized as a type of immune response that directs immune systemcomponents to the site of injury or infection and is a major contributor to many diseases. Inflammation can be localized to a wound or an injury site and it can be systemic. Recent studies show a possible link between cardiovascular diseases andinflammation, e.g., the levels of C-reactive polypeptide, a molecular marker of inflammation, rank with cholesterol levels as indicators of future coronary heart disease. In one aspect, the present invention relates to the use of the compositions herein including for example (i) polypeptides comprising, consisting essentially of, or consisting of, an amino acid sequence such as any one or more of SEQ ID NOs:1-349, or any one or more of SEQ ID NOs: 1-14, 50-244, 248-249, 257-349, or SEQ ID NO: 1; (ii) nucleic acids encoding any of the above polypeptides; (iii) antibodies that specifically bind any of the above polypeptide; and (iv) small molecules or analogsof the above polypeptides. In some embodiments, the compositions above can be used in combination with one or more other anti-inflammatory agents to relieve the inflammation. 4. Neoplastic Growth Cell division and growth are essential for development and repair of organs and tissues. However excessive or uncontrolled growth is an important cause of diseases such as cancer. Endogenous opioid peptides have played a role in regulatingimmunity and tumor growth. In addition to their use in the treatment of pain, opioids appear to be important in the growth regulation of normal and neoplastic tissue (Rasmussen et al., 2002, NEL. 23:193-198). For example, release of endogenous opioidshas been found to stimulate growth of breast cancer in rats and opiate receptor antagonists have reduced the growth of these tumors (Balslev et al., 1989, Am. J. Path., 134:473-479). In another example, cyclooxygenase-2 (COX-2) and the prostaglandinsresulting from its enzymatic activity have also been shown to play a role in modulating cell growth and development of human neoplasia. Evidence includes a direct relationship between COX-2 expression and cancer incidence in humans and animal models,increased tumorigenesis after genetic manipulation of COX-2, and significant anti-tumor properties of NSAIDs in animal models and in some human cancers. Moreover, recent data showed that COX-2 and the derived prostaglandins are involved in control ofcellular growth, apoptosis, and signal through a group of nuclear receptors named peroxisome proliferator-activated receptors (PPARS; Trifan and Hla, 2003, J. Cell. Mol. Med. 7:207-222; Martinsgreen et al., 1994, Cancer Res. 54-4334-4341). Thus, any of the compositions herein can also be used for the treat, prevent or modulate aberrant cell growth and in particular, cancer. Non-limiting examples of cancers that may be modulated, treated, or prevented by the compositions herein include, but are not limited to, breast cancer, skin cancer, bone cancer, prostate cancer, liver cancer, lung cancer, brain cancer, cancer ofthe larynx, gallbladder, pancreas, rectum, parathyroid, thyroid, adrenal, neural tissue, head and neck, colon, stomach, bronchi, kidneys, basal cell carcinoma, squamous cell carcinoma of both ulcerating and papillary type, metastatic skin carcinoma,osteosarcoma, Ewing's sarcoma, reticulum cell sarcoma, myeloma, giant cell tumor, small-cell lung tumor, gallstones, islet cell tumor, primary brain tumor, acute and chronic lymphocytic and granulocytic tumors, hairy-cell leukemia, adenoma, hyperplasia,medullary carcinoma, pheochromocytoma, mucosal neuronms, intestinal ganglioneuromas, hyperplastic corneal nerve tumor, marfanoid habitus tumor, Wilm's tumor, seminoma, ovarian tumor, leiomyoma tumor, cervical dysplasia and in situ carcinoma,neuroblastoma, retinoblastoma, soft tissue sarcoma, malignant carcinoid, topical skin lesion, mycosis fungoide, rhabdomyosarcoma, Kaposi's sarcoma, osteogenic and other sarcoma, malignant hypercalcemia, renal cell tumor, polycythermia vera,adenocarcinoma, glioblastoma multiforme, leukemias, lymphomas, malignant melanomas, epidermoid carcinomas, and other carcinomas and sarcomas. The largest class of tumors falls into the ectoderm/endoderm class. This class includes the leading causes of death in humans (bronchogenic carcinoma, colon adenocarcinoma, breast carcinoma and prostate carcinoma and the most frequentlyoccurring (though usually non-lethal) tumors of humans (squamous cell carcinoma of skin and basal cell carcinoma of skin). The other tumor groups are tumors of mesodermal lineage (including all sarcomas) and tumors of neuroectodermal lineage. Thus, in some embodiments, a composition herein (e.g., SEQ ID NO: 1) can be administered to a subject susceptible of or having cancer to treat, modulate, or prevent the condition. Such compositions include for example (i) polypeptidescomprising, consisting essentially of, or consisting of, an amino acid sequence such as any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or any one or more of SEQ ID NOs: 1-14, 50-244, 257-349, or any one ormore of SEQ ID NOs: 1, 153, 304-349 or any one or more of SEQ ID NO: 1; (ii) nucleic acids encoding any of the above polypeptides; (iii) an antibody or antibody fragment that specifically binds any of the above polypeptide, for the treatment ofinflammatory conditions; and (iv) small molecules or analogs of the above polypeptides. Such compositions can be administered along with one or more anti-neoplastic agents or be co-formulated with one or more anti-neoplastic agents to increase their therapeutic effect. Anti-neoplastic agents can be grouped into the following general categories: alkylating agents, anti-metabolites, mitotic inhibitors, anti-neoplastic antibiotics, hormonal agents, and miscellaneous. Example for an alkylating agent isMechlorethamine hydrochloride that is used to treat Hodgkin's disease in man. Example for antimetabolites is methotrexate, an inhibitor of dihydrofolate reductase. Examples for mitotic inhibitors are Paclitaxel and docetaxel that are antimicrotubuleagents. Examples for antineoplastic antibiotics are Mitoxantrone, an anthracenedione related to the anthracycline antibiotics, Doxorubicin and Bleomycin. Examples for hormonal agents are glucocorticoids. Additional examples of anti-neoplastic agents include, but are not limited to: Acivicin; Aclarubicin; Acodazole Hydrochloride; Acronine; Adozelesin; Aldesleukin; Altretamine; Ambomycin; Ametantrone Acetate; Aminoglutethimide; Amsacrine;Anastrozole; Anthramycin; Asparaginase; Asperlin; Azacitidine; Azetepa; Azotomycin; Batimastat; Benzodepa; Bicalutamide; Bisantrene Hydrochloride; Bisnafide Dimesylate; Bizelesin; Bleomycin Sulfate; Brequinar Sodium; Bropirimine; Busulfan; Cactinomycin;Calusterone; Caracemide; Carbetimer; Carboplatin; Carmustine; Carubicin Hydrochloride; Carzelesin; Cedefingol; Chlorambucil; Cirolemycin; Cisplatin; Cladribine; Crisnatol Mesylate; Cyclophosphamide; Cytarabine; Dacarbazine; Dactinomycin; DaunorubicinHydrochloride; Decitabine; Dexormaplatin; Dezaguanine; Dezaguanine Mesylate; Diaziquone; Docetaxel; Doxorubicin; Doxorubicin Hydrochloride; Droloxifene; Droloxifene Citrate; Dromostanolone Propionate; Duazomycin; Edatrexate; Eflornithine Hydrochloride;Elsamitrucin; Enloplatin; Enpromate; Epipropidine; Epirubicin Hydrochloride; Erbulozole; Esorubicin Hydrochloride; Estramustine; Estramustine Phosphate Sodium; Etanidazole; Ethiodized Oil 1131; Etoposide; Etoposide Phosphate; Etoprine; FadrozoleHydrochloride; Fazarabine; Fenretinide; Floxuridine; Fludarabine Phosphate; Fluorouracil; Fluorocitabine; Fosquidone; Fostriecin Sodium; Gemcitabine; Gemcitabine Hydrochloride; Gold Au 198; Hydroxyurea; Idarubicin Hydrochloride; Ifosfamide; Imofosine;Interferon Alfa-2a; Interferon Alfa-2b; Interferon Alfa-n1; Interferon Alfa-n3; Interferon Beta-1a; Interferon Gamma-1b; Iproplatin; Irinotecan Hydrochloride; Lanreotide Acetate; Letrozole; Leuprolide Acetate Liarozole Hydrochloride; Lometrexol Sodium;Lomustine; Losoxantrone Hydrochloride; Masoprocol; Maytansine; Mechlorethamine Hydrochloride; Megestrol Acetate; Melengestrol Acetate; Melphalan; Menogaril; Mercaptopurine; Methotrexate; Methotrexate Sodium; Metoprine; Meturedepa; Mitindomide;Mitocarcin; Mitocromin; Mitogillin; Mitomalcin; Mitomycin; Mitosper; Mitotane; Mitoxantrone Hydrochloride; Mycophenolic Acid; Nocodazole; Nogalamycin; Ormaplatin; Oxisuran; Paclitaxel; Pegaspargase; Peliomycin; Pentamustine; Peplomycin Sulfate;Perfosfamide; Pipobroman; Piposulfan; Piroxantrone Hydrochloride; Plicamycin; Plomestane; Porfimer Sodium; Porfiromycin; Prednimustine; Procarbazine Hydrochloride; Puromycin; Puromycin Hydrochloride; Pyrazofurin; Riboprine; Rogletimide; Safingol;Safingol Hydrochloride; Semustine; Simtrazene; Sparfosate Sodium; Sparsomycinl, Spirogermanium Hydrochloride; Spiromustine; Spiroplatin; Streptonigrin; Streptozocin; Strontium Chloride Sr 89; Sulofenur; Talisomycin; Taxane; Taxoid; Tecogalan Sodium;Tegafur; Teloxantrone Hydrochloride; Temoporfin; Teniposide; Teroxirone; Testolactone; Thiamiprine; Thioguanine; Thiotepa; Tiazofurin; Tirapazamine; Topotecan Hydrochloride; Toremifene Citrate; Trestolone Acetate; Triciribine Phosphate; Trimetrexate;Trimetrexate Glucuronate; Triptorelin; Tubulozole Hydrochloride; Uracil Mustard; Uredepa; Vapreotide; Verteporfin; Vinblastine Sulfate; Vincristine Sulfate; Vindesine; Vindesine Sulfate; Vinepidine Sulfate; Vinglycinate Sulfate; Vinleurosine Sulfate;Vinorelbine Tartrate; Vinrosidine Sulfate; Vinzolidine Sulfate; Vorozole; Zeniplatin; Zinostatin; and Zorubicin Hydrochloride. 5. Innate Immune System An organism has inborn defense mechanisms or innate immune system that allows it to defend itself against invasions by pathogens. The compositions herein can also be used to modulate, prevent and/or treat pathogen invasions (bacteria, virus, andfingi, crop pests, etc.) in humans and plants. In humans, the few microbes that manage to cross the barriers of skin, mucus, cilia, and pH are usually eliminated by the innate immune system, which commences immediately upon pathogen entry. If phagocytosis cannot rapidly eliminate pathogen,inflammation is induced with the synthesis of cytokines and acute phase polypeptides. This early-induced response is not antigen-specific. Only if the inflammatory process is unsuccessful at eliminating pathogen, the adaptive immune system isactivated. Plants also possess the mechanism of self-defense against pathogens and other abiotic stresses (Cohen et al., (2001) Curr. Opin. Immunol. 13:55-62). Salicylic acid plays an important role in the induction of resistance to a broad spectrum ofwidely different pathogens such as fungi, bacteria or viruses such as the bacteria Pseudomonas syringae and the tobacco mosaic virus (TMV). While conventional pesticides target the pathogens, most non-conventional pest control chemicals (biopesticides)are based on small molecule production either by added genetic material or microorganisms, which increases a plants ability to fight pathogens. Thus, in some embodiments, the compositions herein are used to increase a seed, plant (e.g., crop) or plant cuttings' innate immune response to pathogen (e.g., bacteria, viruses, fungi, crop pests). This can help reduce crop losses. Otherexamples of conditions that may result in crop losses that can be preventable or diminished by the compositions herein include stress conditions such as drought, freezing or reduced temperatures, and other unfavorable environmental conditions (seediscussion of temperature regulation above). Examples of plants that may be treated with the compositions herein include, culture plans such as wheat, barley, rye, oats, rice, sorghum and the like; including Chenopodiaceae, e.g., sugar beet and fodder beet; pome and stone fruits andberries, e.g., apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries and blackberries; Legume, e.g., beans, lentils, peas, soy beans; Brassicaceae, e.g., rape, mustard, cabbages and turnips. Cucurbitaceae, e.g., pumpkins, gherkins,melons, cucumbers, squashes; fibrous plants, e.g., cotton, flax, hemp, jute; citrus fruits, e.g., orange, lemon, grapefruit, mandarin; vegetables, e.g., spinach, lettuce, asparagus, ground-nuts; carrots, onions, tomatoes, potatoes, hot and sweet peppers;laurel-like plants, e.g., avocado, cinnamon, camphor tree; or plants such as maize, tobacco, nuts, coffee, sugar-cane, tea, vines, hops, bananas, rubber plants, poppy, olive, sunflower, coconut, castor-oil plant, cocoa as well as ornamental plants, e.g.,flowers, shrubs, deciduous trees and evergreen trees such as conifers. This list is given with the purpose of illustrating the invention and not to delimiting it thereto. Thus, in some embodiments, a composition herein can be administered to a plant or animal to prevent or treat a pathogen invasion. Such compositions include for example (i) polypeptides comprising, consisting essentially of, or consisting of, anamino acid sequence such as any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or any one or more of SEQ ID NOs: 1-14, 50-244, 257-349, or any one or more of SEQ ID NOs: 1, 153, 304-349 or any one or more ofSEQ ID NO: 1; (ii) nucleic acids encoding any of the above polypeptides; (iii) an antibody or antibody fragment that specifically binds any of the above polypeptide, for the treatment of inflammatory conditions; and (iv) small molecules or analogs of theabove polypeptides. Such compositions can further include a veterinary excipient, pharmaceutical excipient or agricultural excipient. 6. Neurological Condition The present invention contemplates treating or preventing a neurological and/or nuerodegenerative condition using one or more of the compositions herein. Such compositions include for example (i) polypeptides comprising, consisting essentiallyof, or consisting of, an amino acid sequence such as any one or more of SEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or any one or more of SEQ ID NOs: 1-14, 50-244, 257-349, or any one or more of SEQ ID NOs: 1, 153,304-349 or any one or more of SEQ ID NO: 1; (ii) nucleic acids encoding any of the above polypeptides; (iii) an antibody or antibody fragment that specifically binds any of the above polypeptide, for the treatment of inflammatory conditions; and (iv)small molecules or analogs of the above polypeptides. Examples of neurological and neurodegenerative conditions that may be modulated, treated, or prevented by the compositions herein include, but are not limited to, anxiety disorder, panic disorder, obsessive-compulsive disorder, post-traumaticstress disorder, social phobia (or social anxiety disorder), specific phobias, and generalized anxiety disorder. Any of the above conditions can also be accompanied by or manifested by other conditions such as depression, drug abuse, alcoholism, Aicardisyndrome, Alzheimer's disease, amnesia, amyotrophic lateral sclerosis (Lou Gehrig's disease), anencephaly, aphasia, arachnoiditis, Arnold Chiari malformation, Batten disease, Bell's Palsy, brachial plexus injury, brain injury, brain tumors, Charcot-MarieTooth disease, dystonia, encephalitis, epilepsy, essential tremor, Guillain-Barre syndrome, hydrocephalus, hyperhidrosis, Krabbes disease, leukodystrophy, meningitis, Moebius syndrome, multiple sclerosis, muscular dystrophy, Parkinson's disease,peripheral neuropathy, postural orthostatic tachycardia syndrome, progressive supranuclear palsy, prosopagnosia, shingles, Shy-Drager syndrome, spasmodic torticollis, spina bifida, spinal muscular atrophy, stiff man syndrome, synesthesia, syringomyelia,thoracic outlet syndrome, tourette syndrome, toxoplasmosis, and trigeminal neurolagia. For example, a composition comprising a polypeptide comprising any one or more of SEQ ID NOs: 1-349 or a small molecule thereof, or a nucleic acid encoding the above can be used to treat a neurological and/or nuerodegenerative condition such asAlzheimer's disease. Polymorphs, salts, metabolites, and prodrugs of the above are also contemplated herein. 7. Addiction Any of the compositions herein can also be used to treat an addiction in an animal. Such compositions include for example (i) polypeptides comprising, consisting essentially of, or consisting of, an amino acid sequence such as any one or more ofSEQ ID NOs: 1-349 or any one or more of SEQ ID NOs: 1-244, 248-249, 257-349, or any one or more of SEQ ID NOs: 1-14, 50-244, 257-349, or any one or more of SEQ ID NOs: 1, 153, 304-349 or any one or more of SEQ ID NO: 1; (ii) nucleic acids encoding any ofthe above polypeptides; (iii) an antibody or antibody fragment that specifically binds any of the above polypeptide, for the treatment of inflammatory conditions; and (iv) small molecules or analogs of the above polypeptides. In some cases, a composition comprising SEQ ID NOs: 1 or 153, or a small molecule thereof is used to treat an addiction. Such addiction can be an addiction to Morphine for example. In some cases, the composition further comprises one or more antagonists or is co-administered simultanesouly or at a different time with an antagonist such as an opioid anagonists. Examples of antagonists include those selected from the group consisting of Alvimopan, trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine; ANTI, 5'-acetamidinoethylnaltrindole; 4-Aminoquinoline;N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamide monohydrochloride; Benzimidazolinone; 7-Benzylidenenaltrexone; Binaltorphimine; nor-Binaltorphimine; Butorphanol (17-cyclobutylmethyl-3,14-dihydroxymorphinan) tartrate; CTAP,D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2; CTOP, D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr-NH2 (SEQ ID NO: 32); Cyclazocine; Cyprodime; 1,3-Dimethyl-4-piperidinone; Ethylketocyclazocine; β-Funaltrexamine; GNTI, 5'-Guanidinonaltrindole; ICI 174864,N,N-diallyl-Tyr-Aib-Aib-Phe-Leu (SEQ ID NO: 40); Indolomorphinan; 5 -Isothiocyanate; J-113397, 1-[(3R,4R)-1-Cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1,3-di- hydro-2H-benzimidazol-2-one; JDTic,(3R)-7-Hydroxy-N-[(1S)-1-[[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dimethyl-1-pip- eridinyl]methyl]-2-methylpropyl]-1,2,3,4-tetrahydro-3-isoquinoline-carboxa- mide 3-Quadazocine; Loperamide; Methoxynaltrexone; Methylnaltrexone; Mr 2266; Nalmefene; Nalorphine;Naloxone; Naloxone methiodide; Naloxazone; Naltrexone; β-Naltrexamine; Naltriben; Naltrindole; Phenylpiperidine; SB-612111, (-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9- -tetrahydro-5H-benzocyclohepten-5-ol; SoRI 9409,59-(4-chlorophenyl)-17-(cyclopropylmethyl)-6,7-didehydro-3,14-dihydroxy-4- ,5a-epoxypyrido-[29, 39:6,7]morphinan, SNC 80; TIPP-y, Tyr-Tic-Phe-Phe; Triethyleneglycolnaltrexamine. The antagonist can be co-formulated with the compositions herein or co-administered (administered separately). Non-limiting examples of addictions that can be treated (prevented, reduced, or cured) using the methods herein include alcoholism, addiction to cocaine, addiction to morphine, addiction to heroine, and addiction is to a painkiller. 8. Modulating Opioid Receptor/Opioid Receptor-Like The compositions herein are used to modulate the production (e.g., expression) or effects of one or more opioid receptor (e.g., μ, κ, and/or δ). Modulation of opioid receptors can be used to regulate (e.g., downregulate orupregulate) cellular signaling via the enzyme adenylyl cyclase and via ion channels. For example, the activation of all three opioid receptors inhibits adenylyl cyclase and modulates membrane conductances of Ca2 and K.sup. (Childers (1993)Handbook of experimental pharmacology: opioids I, Vol 104 (Herz A, ed), pp 189-216. Berlin: Springer; North (1993) Handbook of experimental pharmacology: opioids I, Vol. 104, pp, 773-797). The receptors also affect respiration, gastrointestinalfunction, blood pressure, immunoregulation, and thermoregulation. Thus, any of the compositions herein (including the polypeptides and nucleic acids herein) can modulate these effects. In some cases, the compositions herein are used to regulate a receptor of aspirin (ASA). As such, the compositions herein can be used as a substitute for aspirin or for screening for novel compounds that are useful as substitutes for aspirin. For example, the compositions herein (polypeptides disclosed herein or nucleic acids thereof can be used for antiplatelet and/or anti-inflamatory therapy. The compositions herein can also be used to reduce prostaglandin (PG) formation, therapy tocardiovascular diseases, prevention of acetylation of cyclooxygenase 1 (COX-1), neuroprotection of infarcts after ischaemic stroke, protection against glutamate neurotoxicity. The compositions herein can also be used to modulating aspirin receptor(s)which in turn reduces the recurrence of colorectal adenoma (Martinez et al., (2003) Proc. Nat. Acad. Sci. 100:7859-7864), lower breast cancer risk (Terry et al., (2004) JAMA 291:2433-2440), and function as a chemopreventive agent against colon cancer(Quyang et al., Carcinogenesis (2006) 27:232:239). Screening Assays The present invention also contemplates screening assays designed to identify agents that alter (e.g., increase or decrease in a statistically significant manner) one or more of the compositions herein (e.g., a polypeptide comprising, consistingessentially of, or consisting of an amino acid sequence of (or encoded by) SEQ ID NOs: 1-349, or any of the above with a methionine at the N-terminus). The present invention also contemplates screening assays that identify small molecules or analogs ofthe compositions herein (e.g., any one of SEQ ID NOs: 1-349). Finally, the present invention contemplates assays that identify targets of the compositions herein (e.g., SEQ ID NOs: 1-349). For example, in certain embodiments, when the compositions herein are contacted with a known polypeptide in the absence and presence of a candidate agent and under conditions and for a time sufficient for binding to the polypeptide to occur, andthe effect of the agent on the binding interaction between the polypeptide and a composition herein is determined. A candidate agent may alter any of the herein described parameters directly (e.g., by physical contact with the polypeptide at a site ofligand binding) or indirectly (e.g. by interaction with one or more proximal or distal sites within the polypeptide, as may according to non-limiting theory alter the described parameter by interacting with other than a site of ligand binding, forinstance, electron transfer or UV absorbance, or changing the conformation of the polypeptide). In some embodiments, the candidate agent may be a peptide, polypeptide, polypeptide or small molecules, and in certain preferred embodiments the candidateagent may be a structural mimetic of one or more of the compositions herein. Typically, and in more preferred embodiments such as for high throughput screening, candidate agents are provided as "libraries" or collections of compounds, compositions ormolecules. Such molecules typically include compounds known in the art as "small molecules" and having molecular weights less than 104 daltons, preferably less than 105 daltons. For example, members of a library of test compounds can beadministered to a plurality of samples, each containing at least one homolog of a polypeptide herein and a known polypeptide as provided herein, and then assayed for their ability to alter at least one of the above-described parameters. In another example, small molecules are screened to identify ones that interact with or mimic (have similar 3D structure) any one or more of SEQ ID NOs: 1-349. Candidate agents can be provided as members of a combinatorial library, whichpreferably includes synthetic agents prepared according to a plurality of predetermined chemical reactions performed in a plurality of reaction vessels. For example, various starting compounds may be prepared employing one or more of solid-phasesynthesis, recorded random mix methodologies and recorded reaction split techniques that permit a given constituent to traceably undergo a plurality of permutations and/or combinations of reaction conditions. The resulting products comprise a librarythat can be screened followed by iterative selection and synthesis procedures, such as a synthetic combinatorial library of peptides. Those having ordinary skill in the art will appreciate that a diverse assortment of such libraries may be preparedaccording to established procedures, and tested using the known polypeptides as a target. There are a variety of assay formats known to those of ordinary skill in the art for detecting binding interactions between polypeptides and their cognate ligands (See, e.g., Harlow and Lane, 1988 In: Antibodies: A Laboratory Manual, Cold SpringHarbor Laboratory). Within one embodiment, a polypeptide or polypeptide is immobilized on a solid support prior to contact with the ligand. Binding may then be detected using a detection reagent that specifically binds to the polypeptide, for example,at a site known or suspected of being a site of ligand interaction (e.g., an antibody or fragment thereof), or using a detectable portion of the polypeptide (e.g., direct detection of a UV-absorbing moiety, or detection of electron transfer to anacceptor molecule). A solid support may be any material known to those of ordinary skill in the art. For example, the solid support may be a test well in a microtiter plate or a nitrocellulose or other suitable membrane. Alternatively, the support may be a bead ordisc, such as glass, fiberglass, latex or a plastic material such as polystyrene or polyvinylchloride. A polypeptide may be immobilized on the solid support using a variety of techniques known to those of skill in the art, which are amply described inthe patent and scientific literature. In the context of the present invention, the term "immobilization" refers to both non-covalent association, such as adsorption, and covalent attachment (which may be a direct linkage between the agent and functionalgroups on the support or may be a linkage by way of a cross-linking agent). Immobilization by adsorption to a well in a microtiter plate or to a membrane is preferred. In such cases, adsorption may be achieved by contacting the binding agent, in asuitable buffer, with the solid support for a suitable amount of time. Binding is generally allowed to occur under solution conditions and for an amount of time sufficient to detect the bound ligand. An appropriate amount of time may generally be determined by assaying the level of binding that occurs over a periodof time. After incubating under conditions and for a time sufficient to permit interaction of a polypeptide of the invention and candidate receptor agent, the level of the ligand-receptor binding is detected and compared to the level of binding in thepresence and absence the polypeptide of the invention. For example, following a suitable interval for competitive ligand binding, unbound ligand is removed, and bound ligand is detected using a linked reporter group or a separate detectable marker comprising a reporter group. The method employed fordetecting binding depends upon the nature of the reporter group employed. When electron transfer is detected, fluorescence or colorimetric or other techniques may be used. For radiometric quantification of ligand binding (or, e.g., competitiveinhibition by a candidate agent of the binding site for a polypeptide comprising, consisting essentially of, or consisting of an amino acid sequence of (or encoded by) any one or more SEQ ID NOs: 1-349, or any of the above with a methionine at theN-terminus, of a detectably labeled ligand comprising a radioactive group), scintillation counting or auto-radiographic methods are generally appropriate. Spectroscopic methods may be used to detect dyes, luminescent groups and fluorescent groups. Biotin may be detected using avidin, coupled to a different reporter group (commonly a radioactive or fluorescent group or an enzyme). Enzyme reporter groups may generally be detected by the addition of substrate (generally for a specific period oftime), followed by spectroscopic or other analysis of the reaction products. An agent that binds to a polypeptide of the invention and/or to a polypeptide complex comprising a polypeptide of the invention may result in a detectable decrease or increase in binding the polypeptide to its natural receptor. Such alteredlevels of ligand-receptor binding can be detected by a statistically significant increase or decrease in binding to the receptor. Such agents that interfere with the ligand-receptor binding may be used as inhibitors of the compositions herein. One or more of above peptides can be used to screen small molecules and other compounds (e.g., antibodies, peptides, peptide nucleic acids, and nucleic acids) that interact with any one or more of SEQ ID NOs: 1-349. Such library of compounds caninclude at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 40, 50, 60 or 70 agents. The present invention provides compositions, methods and kits for use in a phage display peptide library in which a library of analogs or variants of one or more of SEQ ID NOs: 1-349, is expressed on the outside of a phage virion, and the DNAencoding each variant or analog resides inside the virus. This creates a physical linkage between each variant protein sequence and the DNA encoding it, which allows rapid partitioning based on binding affinity to a given target molecule (antibodies,enzymes, cell-surface receptors, etc.) by an in vitro selection process called panning (Whaley et al., 2000, Nature 405:665-668). The present invention also provides methods for identifying lead compounds for treatment of mitochondrial and metabolic conditions such as pain, inflammation, fever, Alzheimer's disease and any other disease mentioned herein. Such methodsinvolve the use of a thermogenic plant for studying thermoregulation activity by candidate agents. Examples of thermogenic plants include those such as the Sauromatum guttatum, members of the Araceae family, Amorphophallus konjac, Arum italicum, A.dioscoridis, Dracunculus vulgaris; lotus (Nelumbonaceae), Dutchman's pipes (Aristolochiaceae), palms (Arecaceae and Cyclanthaceae), custard apples (Annonaceae), magnolias (Magnoliaceae), Illicium (Illiciaceac), Rafflesia (Rafflesiaceae), winter's bark(Winteraceae) and cycads (Cycadaceae). In one example, using Sauromatum guttatum as the experimental module, on the day of inflorescence-opening, the Sauromatum appendix (a 20-40 cm-long, slender organ) becomes warm, reaching a 32° C. temperature (Skubatz et al., 1991, PlantPhysiol. 95-1084-1088). The heat generated by the appendix is generated by the mitochondria. This mitochondrial activity can be triggered by the addition of phenolic compounds, including but not limited to, salicylic acid, aspirin, and2,6-dihydroxybenzoic acid. Test agents can be applied to the plant and the plant's temperature may be monitored in vivo. Test agents (e.g., polypeptide, such as those disclosed herein) that can modulate (increase, decrease, sustain, or shorten) heat generated by the plants can be used as lead compounds in animal models to test their ability to treat/modulate ametabolic condition. In some embodiments, small molecules or mimetics of the test compounds are applied to the plants. A small molecule or mimetic that has the same effect as a test agent such as a polypeptide may be then tested in an animal model forits ability to treat/modulate a metabolic condition. In some embodiments, such test compounds are agonists, antagonists and/or other modulators of mitochondrial activities. In one embodiment, the present invention contemplates structure-based screening to identify binding sites on the target of any of the peptides herein (e.g., binding site on opiopid receptors). Such screening can be made using, for example, x-raycrystallography and nuclear magnetic resonance spectroscopy. The above techniques can be coupled with combinatorial chemistry to synthesize molecules that have similar or improved binding affinities to the target with optimized efficacy. Administration The compositions (including formulations) herein can be administered systemically or locally to a plant or animal by any means known in the art. For example, to an animal such as a human, the compositions herein can be administered parenterally(which includes subcutaneously, intravenously, intramuscularly, intrasternally, intracavernously, intrathecally, and intraurethrally), intracranially, intraorbitally, intracapsularly, intraspinally, intracistemally, intrapulmonarily (via inhalation),orally, intravenously, intra-arterially, intramedullary, intrathecally, intraventricularly, intrameatally, transdermally, subcutaneously, intraperitoneally, intranasally, enterally, vaginally, sublingually, or rectally. Preferably, the compositionsherein are administered to an animal topically, subdermally or intravenously. In some embodiments, the composition/formulations herein are administered using insert(s), bead(s), timed-release formulation(s), patch(es) or fast-release formulation(s). For plants, the compositions herein can be administered by any method known in the art, including, but not limited to, spray, drip irrigation or other irrigation, dipping at least a portion of said plant or seed in said composition, coating atleast partially said plant or seed with said composition, etc. In another embodiment, a nucleic acid sequence encoding any of the above compositions can be used to transfect plants such that their heat production is regulated. The compositions/formulations herein are preferably administered in an effective dose. It will be evident to those skilled in the art that the number, frequency, and duration of administration will be dependent upon the response of the host. For therapeutic delivery, agents at concentrations of about 0.01 μg/kg to about 1000-mg/kg-body weight may be administered, typically by the intradermal, subcutaneous, intramuscular or intravenous route, or by other routes. A preferred dosageis about 1 μg/kg to about 1000 mg/kg, or about 5 μg/kg to about 500 mg/kg, or about 10 μg/kg to about 100 mg/kg. For agricultural delivery, agents may be administered at a concentration that is agriculturally therapeutically effective, e.g., about 50-3000 grams per hectare, preferably from about 50-1500 gram per hectare, and more preferably from about150-300 gram per hectare. Assuming a composition is comprised of 100% active ingredients, then, in general, the amount of the subject composition used will range from about 0.005% to 25% of the weight of the seed, and more preferably, from about 0.01%to about 10% of the weight of the seed. In yet another embodiment the amount of the subject composition used will be in the range of 0.01% to 1% of the active ingredients relative to the weight of the seed, or 0.05% to 0.5%. EXAMPLES Example 1 A total of forty (40) male Sprague Dawley rats (Harlan Sprague Dawley Inc., Indianapolis, Ind., USA) were used in the study. The rats are specific pathogen free and approximately 250 grams upon arrival. The rats were housed in the vivarium inclear polycarbonate plastic cages (48×27×20 cm); 2 rats per cage until a few days prior to surgery at which point they were singularly housed for the remainder of the study procedures. The bedding material is irradiated corn-cob bedding(Bed-O-Cob, The Andersons, Maumee, Ohio, USA) that was changed weekly. The rats were acclimated for two weeks prior to the commencement of the experimental procedures. The room in which the rats were housed throughout the study was supplied with HEPAfiltered air at the rate of 10-15 air changes per hour. The temperature was maintained at 18-26° C. with a relative humidity of 30-70%. Illumination is approximately 300 lumens/m2 at 1 m above floor level on a 12-hour light/dark cycle. The rats had ad libitum access to oval pellet Certified Picolab Rodent Diet 20 (PMI Feeds Inc., Richmond, Ind., USA) and deionized water. All rats were anesthetized with Inhalation anesthetic (Isoflurane). The plantar aspect of the foot was cleaned and prepped for aseptic surgery. The animals were placed in ventral recumbancy. A 1-246 cm longitudinal incision was made with a #11blade, through the skin and fascia of the plantar aspect of the foot, starting 0.5 cm from the proximal edge of the heel and extending towards the toes. The plantaris muscle was elevated and incised longitudinally. The muscle origin and insertionremained intact. Gentle pressure was applied for hemostatis, if needed. The skin was closed with suture material and the wound site covered with a triple antibiotic ointment. The rats were allowed to recover in their cage until regaining fullmobility. On days 1 and 3 post-surgery, animals were dosed with the appropriate test or control compound (Table III). TABLE-US-00003 TABLE III Treatment groups for the first study of the analgesic property of SEQ ID NO: 1 on post-operative pain in rats. Group No. Surgery Treatment Dose Route 1 Sham Vehicle 0.17% DMSO, 0.1 mL Topical (No surgery) 0.05% Silwetin H2O 2 Brennan model Vehicle 0.1 mL Topical 3 Brennan model Morphine in PBS 5 mg/kg Subcutaneous 4 Brennan model SEQ ID NO: 1 150 μg/0.15 mL Topical in vehicle 5 Brennan model SEQ ID NO: 1 150 μg/0.1 mL Subdermal in PBS On days 1 and 3 post-surgery, the rats underwent Von Frey testing for mechanical allodynia. Tactile sensitivity (i.e. mechanical allodynia) was measured using calibrated filaments touched to the plantar surface of the affected limb. Procedurally, the rats were placed in a plastic cage with a wire mesh bottom and allowed to acclimate for 5 to 10 minutes. Once the animals settled, the plantar surface of the right hind paw was touched with a 2.0 g von Frey filaments. In theabsence of a paw withdrawal response to the initially selected filament, a stronger stimulus was presented; in the event of paw withdrawal, the next weaker stimulus was chosen. In this fashion, the resulting pattern of positive and negative responseswas used to determine the paw withdrawal threshold. FIG. 1. Data were analyzed using a one-way ANOVA followed by Newman-Keuls' Multiple Comparison. Statistical significance was p<0.05. It shows that SEQ ID NO: 1 was able to significantly reduce pain. Abbreviations: TA, test article, whichis SEQ ID NO: 1; sderm, sub-dermal injection; top, topical application; veh, vehicle; surg, surgery; morph, morphine. The rats appeared relaxed and with less anxiety. Example 2 In a second independent study the rat hind paw withdrawal sensitivity was again evaluated after 3 h and 3 day post-surgery when the rats had received SEQ ID NO: 1 at three different concentrations: 1, 15 and 50 mg/kg. The dosing route wassubdermal injection adjacent to the wound site. The rats received one dose 3 hours after the surgery and on Day 3 post-surgery, group 3 was dosed again as described in the Table IV. Pain measurements were taken 15-20 min after application of the drug. Baseline pain behavior was measured as follows: Withdrawal responses to mechanical stimulation were determined using von Frey filaments applied from underneath the cage through openings (12×12 mm in the plastic mesh floor to an area adjacent to theintended incision. Each von Frey filament (Target force of 0.008 g to 300 g) was applied once starting with 0.008 g filament and continuing until a withdrawal response occurred or 300 g force was reached. The median force producing a response,determined from three tests given over a 10-min period was considered the withdrawal threshold. FIG. 2 illustrates withdrawal results show that SEQ ID NO: 1 has analgesic and property 3 b after surgery. In the saline treated animals, the control 3-hour post-surgery were 25.1, 4.4 and 12.7 g, indicating significant hyperalgesic responseimmediately after surgery which subsided by Day-3. In the animals treated with 50 and 15 mg/kg doses of SEQ ID NO: 1 subdermally, the pre-dose, pre-surgery responses were 30.2 and 28.1 g, which were comparable to the saline treated group indicatinguniformity of the pain response in all the three groups. The withdrawal response in the 50 mg/kg SEQ ID NO: 1 administered on Day-1 was 9.9 g compared to the 4.4 g for the saline group at the same time-point, indicating a 125% effect. The dataexpressed as mean. -.SE, were analyzed using ANOVA followed by Tukey-HSD Multiple Comparison Test. Statistical significance was p<0.05. FIG. 3 Withdrawal results show that SEQ ID NO: 1 has analgesic and property on Day 3 post-surgery. The group, which did not receive any further dosing showed a 31% increase in response time on Day 3, compared to the saline group at therespective time point. In the group of animals administered with 1 mg/kg NPL/PA2 on day 1 post-surgery, the 3-hour post surgery measurements showed a 39% increase in the pain threshold. On Day-3, when these animals were administered with 15.25 mg/kg ofSEQ ID NO: 1 subdermally, the withdrawal response was at 21.3 g, compared to the withdrawal response of saline group at 12.7 g, constituting an increase of 68%. The data expressed as mean. -.SE, were analyzed using ANOVA followed by Tukey-HSD MultipleComparison Test. Statistical significance was p<0.05. TABLE-US-00004 TABLE IV Treatment groups for the first study of the analgesic property of SEQ ID NO: 1 on post-operative pain in rats. Number of Concen- Animals Time of tration Group Male Route Dosing (mg/kg) 1 10 saline, Day 1, 3 h after 0vehicle surgery 2 10 subdermal Day 1, 3 h after 50 mg/kg surgery 3 10 subdermal Day 1, 3 h after 1 mg/kg surgery Day 3 15 mg/kg Example 3 An adult male subject suffering from chronic pain as a result from of multiple fractures to both tibia and fibula in both legs and severe traumatic soft tissue damage was topically administered a composition containing a polypeptide of SEQ ID NO:1 at regions experiencing pain (mostly knees and ankles). The pharmaceutical formulation administered comprised of 5 μM of SEQ ID NO: 1 in 0.01% Silwet L-77. Relief was noticed within 15 min. after administration of a single dose of about 5 μg/10cm2 of SEQ ID NO: 1. The relief lasted for more than a week. A scaled score of 1 to 10 was used to evaluate treatment efficacy where a score of 10 represented a patient with sever pain discomfort and complete inability to walk. A scaled score of 1represented a patient experiencing no pain and able to freely walk or move the legs. Prior to treatment, the patient scored an 8-9 representing chronic pain and difficulties in walking long distance. After the treatment, the patient scored a 2-3representing a significant decrease in pain. Treatment efficacy lasted for about 10 days. Example 4 FIG. 4 illustrates modulation of heat generated by aspirin (ASA) in Sauromatum guttatum appendix in the presence of various opioid peptides and the Alzheimer's peptide, Aβ 1-42. One day before heat-production, sections of the appendix wereplaced in different aqueous solutions containing ASA with or without an opioid peptide. [Leu]-Enkephalin, SEQ ID NO: 15; Human β-Endorphin; SEQ ID NO: 19; Dynorphin A, SEQ ID NO: 21; Endomorphin 2, SEQ ID NO: 24; Neuropeptide AF, SEQ ID NO: 44;β-human-Casomorphin, SEQ ID NO: 47; Alzheimer's peptide, SEQ ID NO: 48. Sections of the appendix were placed in distilled water that was not generated any heat is the control (9). Temperature was recorded with thermocouples attached to the sectionevery 5 min. The y-axis is the appendix temperature above ambient and the x-axis shows the time of the day. This figure illustrates that opioid peptides and the neurotoxic Alzheimer's peptide, Aβ 1-42 can modulate thermogenicity in plants as wellas animals and act as mitochondrial modulators. Example 5 FIG. 5 illustrates modulation of heat generated by salicylic acid (SA) in the presence of human opioid peptides (β-Endorphin, SEQ ID NO: 19 and Nueuropeptide AF, SEQ ID NO: 44) and, the Alzheimer's peptide, Aβ 1-42, SEQ ID NO: 49, and,a plant virulent bacterial pathogen (Pst DC3000). One day before heat-production, sections of the appendix were placed in different aqueous solutions containing salicylic acid (SA) with or without a peptide or with the bacterial plant pathogen,Pseudomonas syringae pv. Tomato, DC3000 Sections from the appendix were placed in distilled water that was not generated any heat is the control (water). Temperature was recorded with thermocouples attached to the sections every 5 min. The y-axis isthe appendix temperature above ambient and the x-axis shows the time of the day. This figure illustrates that these peptides modulate thermogenicity in plants as well as animals and act as mitochondrial modulators. Example 6 FIG. 6 illustrates modulation of heat generated by 2,6-dihydroxybenzoic acid in the presence of the Alzheimer's peptide, Aβ 1-42, SEQ ID NO: 49 and a plant gene derived sequence in the Sauromatum guttatum appendix. One day beforeheat-production, sections of the appendix were placed in different solutions containing 2,6-dihydroxybenzoic acid (2,6-DHBA) with or without SEQ ID NO: 2 (FLPSEFGVDVDR) and SEQ ID NO: 51. Heat-production was monitored with thermocouples attached to thesections. A section placed in distilled water that was not generated any heat is the control (water). The y-axis is the appendix temperature above ambient and x-axis shows the time of the day. The temperature was recorded every 5 min. Moreover, in asecond experiment, application of SEQ ID NO: 2 up to 50 μM did not generate heat (data not shown). This figure illustrates that these peptides modulate thermogenicity in plants as well as animals and act as mitochondrial modulators. Example 7 Administration of 10 μm of SEQ ID NO: 1 in 0.01% Silwet L-77 to Arabidopsis thaliana plants induces early flowering and abundance of flowers and pods. Example 8 Seeds of Arabidopsis ecotype Columbia (Col-0) were planted in potting soil. Plants were cultivated in a growth chamber with 10-h d (200 μmol m-2s.sup.-1 at 22° C.) and 14-h night (18° C.) cycles and 80% RH. Once a weekplants were supplied with water and modified one-half strength Hoagland nutrient solution: 2 mM KNO 5 mM Ca(NO3)2 and trace elements, pH 7. A virulent plant pathogen, Pst Pseudomonas syringae pv tomato, DC3000 was grown at 28° C. on King's medium B containing 40 mg/L tetracycline. Plants were inoculated with 1×107 cfu/ml of the pathogen in 0.01% Silwet L77 (v/v)(a surfactant) and distilled water 5 weeks after sowing. The bacterial suspension or a control solution (0.01% Silwet L77 in water) was then sprayed on the plant once. Disease symptoms in Arabidopsis are water-soaked, spreading lesions, sometimes surrounded by chlorotic margin that eventually lead to yield loss and plant death. To test the efficacy of SEQ ID NO: 15, some healthy and some disease plants were sprayed with salicylic acid in 0.01%. Silwet L77; some healthy and some disease plants were sprayed with SEQ ID NO: 15 in 0.01%. Silwet L77, and some healthy andsome disease plants were sprayed with salicylic acid in combination with SEQ ID NO: 15 in 0.01%. Silwet L77. A control group of some healthy and some disease plants were sprayed with water in 0.01%. Silwet L77. Symptoms of plants were classified by the percentage of infected leaves and the severity of the infection. It was noted that application of 20 μl salicylic acid at a concentration of 1 mM and 20 μl SEQ ID NO: 15 to the leaves is enough to trigger systemic resistance to the virulent bacteria concentration. Example 9 Original of Peptides The human preprodynorphin is encoded by the PYND gene known also as preproenkephalin B gene (Horikawa et al. 1983). The 28-kD precursor, preprodynorphin, is post-translationally cleaved to form 5 secreted opioid peptides: beta-neoendorphin,dynorphin, leu-enkephalin, rimorphin, and leumorphin. The precursor consists of 254 aa with a signal sequence (region 1-20 aa) that precedes a conserved region of about 50 residues; a variable-length region; and the sequence of the neuropeptides(Beta-neoendorphin, 175-183; Dynorphin 207-223; Leumorphin, 226-254; Rimorphin, 226-238; Leu-enkephalin 226-230). These peptides are ligands for the kappa-type of opioid receptor. SEQ ID NO: 1 identified herein is residues 91-94 in the variable region. This region does not contain any known active peptides. Incision activates the nociceptive system as a result of receptor stimulation by tissue injury. A reduction in the threshold of the nociceptors that transfer input from peripheral targets (skin, muscle, joints and the viscera) to the spinal cordand CNS causes the pain perception in the brain (Treede 1995; Brennan 1999). It has been shown that the receptive fields of dorsal horn neurons develop exaggerated responses to mechanical stimuli after plantar incision (Brennan 1999; Zahn et al. 2002). This pain is usually time limited and when the tissue damage heals, the pain typically resolves. Examples of noniceptive pain are: inflammation (from an infection or arthritic disorder), sprains, bone fractures, burns, bumps, bruises, and obstructions,and myofascial pain and they respond well to treatment with opioids. Since the peptide affects the wounded area at very low concentrations, it is conceivable that it exerts it effects on the periphery and possibly on the brain. Peripheral opioid receptors are not active in normal tissue but become so withinminutes to hours at the onset of inflammation (Stein 1995; Schafer 1999; Wenk & Honda 1999). It seems that their activity is due to high level of μ-opioid receptor mRNA (Schafer 1999) and mu-opioid binding sites (Stein 1995; Stein et al. 2003). These facts have demonstrated that opioid receptors are present on sensory nerve terminals before inflammation begins. Thus, peripheral opioid effects must be due to some mechanisms induced by the inflammatory process. Recent studies indicate thatopioids gain easier access to neuronal opioid receptors during inflammation because of disruption of the perineurium, an impermeable sheath encasing peripheral nerve fibers (Schafer 1994). Further, the number of opioid receptors on cutaneous nervefibers in the inflamed footpad also increases over several days (Stein 1993). These studies demonstrate that inflammation stimulates the axonal transport of opioid receptors to the periphery and increases their number (up-regulation) on peripheral nerveterminals. The endogenous ligands of peripheral opioid receptors are opioid peptides (endorphin, enkephalin, dynorphin) that have been detected in immune cells within inflamed tissue of animals and humans (Stein 1990, 1993). These opioid peptides occupytheir receptors during chronic persistent inflammation. Pain is basically managed by two classes of drugs. The NSAIDs that block the pain-causing COX enzymes and narcotics, which are the most effective drugs for pain, act on the brain. The peptide has no anti-inflammatory properties and thisdifferentiates it pharmacologically from analgesics in the NSAID's. The exposure of rats to high levels of the peptide did not invoke an abnormal feeding behavior for at least 3 days. Clearly it does not adversely affect brain function under theseconditions. NSAIDs are in general well tolerated but can induce gastric bleeding and even stroke and heart attack. It is administered orally or topically whereas narcotics are administered systemically and their downside is severe side effects. There isgrowing evidence that some narcotics can be applied peripherally (Stein 1993). Opioid peptides are administrated directly to the spinal cord but their use is limited because of their short lasting effects, sometimes only a few min. However, some can be given subcutaneously e.g., [Dmt1]DALDA (Neilan 2001; Schiller 2005) orare administrated systemically and get into the brain (Weber et al. 1991). Their metabolism and clearance from the body is complete different routes than small molecules. For example, the liver Cyt P450 is not involved in their breakdown, thus livertoxicity is not an issue. The peptides are degraded by cellular proteases. Peptides at this size (less than 500 Dalton) on one hand lack immunogenicity but on the other hand can be very potent. The novel peptide may have all the benefits of peptide drugs with high specificity to a specific receptor. A topical application of this peptide analgesic lowers the risk of unforeseen side effects and the small amount needed makes thisapplication safe. Furthermore, its ability to increase the baseline threshold for pain can be used in local anesthetic to block nerve impulses. Example 10 The study was conducted with 2 groups of 10 male Sprague Dawley rats, 5-6 weeks old. The rat is a standard species used for the evaluation of potential analgesic properties of a test article. The rats were anesthetized and subjected to asurgical incision to the plantar surface of the right hind paw. Rats were administered the 0.9% saline or SEQ ID NO: 1 at 100 mg/kg 3 hours after surgery and tested for pain responses using von Frey filaments through openings in the cage floor 15-20minutes later on Day 1 and again on Day 3. The test article was SEQ ID NO: 1, a white powder, which was delivered in 0.9% saline. The test article formulations were prepared on the day of study and kept at room temperature until dosing. 100 mg/kg at 1 mL/kg=100 mg/mL 1.4 mL of salineadded to 141.5 mg of test article, soluble. Rats were group housed in a room with 12 hour light/12 hour dark at a temperature of 18.9 to 22.2° C. All animals had access to Harlan Teklad Rodent Diet (certified) ad libitum except during fasting. No contaminants were known to be present in the certified diet at levels that would be expected to interfere with the results of this study. Tapwater was available ad libitum, to each animal, via an automatic watering device. No contaminants were known to be present in the water at levels that would be expected to interfere with the results of this study. Study animals were acclimated to theirhousing for 6 days prior to their first day of dosing. All animals received for this study were assessed as healthy prior to initiation of the study. Rats were randomly assigned to study groups. The group assignment and dose levels received by each group are illustrated in the table V below. TABLE-US-00005 TABLE V Group Assignments and Dose Levels Number of Volume Animals Dose Injected Group Male Drug (mg/kg) (mL/kg) 1 10 Vehicle 0 1 Sterile saline 2 10 SEQ ID Day 1 1 NO: 1 (100 mg/kg) Dosing was administered by subdermal injection adjacent to the wound site 3 hours after the surgery. Each animal received a bolus dose at 1 mL/kg as described in the table. Animals were weighed, and placed in groups. Animals were anesthetized with 1.8 to 4% isofluorane (delivered via a nose cone) and each received an intramuscular injection of penicillin (30,000 IU) in the triceps muscle after preparation of thefoot with betadine and alcohol (SOPs VET-1 and VET-8). A 1 cm long incision of the skin and fascia was made in the plantar aspect (heel, midfoot or distal pad area) of the right hind paw. No underlying muscle was incised. After hemostasis with gentlepressure, the incision was closed with one or two sutures (5-0 silk suture on a taper TF needle). The wound site was covered with a mixture of polymixin B, neomycin, and bacitracin ointment. After surgery, rats were allowed to recover in their cagesuntil behavioral testing. Before the experiment, the rats were placed individually on an elevated plastic mesh floor covered with a clear plastic cage top and allowed to acclimate. Baseline pain behavior was measured as follows: Withdrawal responses tomechanical stimulation were determined using von Frey filaments applied from underneath the cage through openings (12×12 mm in the plastic mesh floor to an area adjacent to the intended incision). Each von Frey filament (Target force of 0.008 g to300 g) was applied once starting with 0.008 g filament and continuing until a withdrawal response occurred or 300 g force was reached. The median force producing a response, determined from three tests given over a 10-min period, was considered thewithdrawal threshold. Rats were tested for responses on the day of surgery, 15-20 min after application of the drug and 3 days post-surgery. The test article/vehicle was administered 3 hours after surgery and pain measurements were taken 15-20 minafter application of the drug. Rats were euthanized after the measurements were taken on Day 3. Using Systat v.9.01 software, the data was analyzed by an unpaired t test to compare the vehicle control and the test article groups. Statistical significance was accepted if p≤0.05. In the saline treated animals, the predose, 3 hour post-surgery and Day 3 post-surgery responses were 34.0, 4.2 and 15.7 g, indicating significant hyperalgesic response immediately after surgery which subsided by Day-3. In the animals treated with SEQ ID NO: 1 at 100 mg/kg subdermally, the pre-dose, pre-surgery responses were 32.5 g, which was comparable to the saline treated group indicating uniformity of the pain response in both of the groups. As presented in FIG. 7, the withdrawal response in the 100 mg/kg SEQ ID NO: 1 administered group on Day 1 was 52.7 g compared to the 4.2 g for the saline group at the same time-point, indicating a 1,155% effect which was statistically significant(p≤0.05) compared to the saline treated group. On Day 3, the withdrawal response for the SEQ ID NO: 1 group was 19.3 g, which was comparable to the withdrawal response of 15.7 g observed in the saline group (FIG. 8). In this assay, SEQ ID NO: 1 administered subdermally at a dose of 100 mg/kg produced a statistically significant (analyzed by unpaired t test) increase in pain threshold in the Brennan model of post-incisional pain in rats. Example 11 Table VI below illustrates results from the oral administration of SEQ ID NO: 1 and SEQ ID NO: 153 and the effects of Naloxone and aspirin on their ability to decrease the pain threshold. In this experiment animals were weighed and placed in the group numbers designated on the left hand column. Each group is composed of 10 rats. Animals were anesthetized with 1.8 to 4% isofluorane (delivered via a nose cone) and each received anintramuscular injection of penicillin (30,000 IU) in the triceps muscle after preparation of the foot with betadine and alcohol (SOPs VET-1 and VET-8). A 1 cm long incision of skin and fascia was made in the plantar aspect (heel, midfoot or distal padarea) of the right hind paw. No underlying muscle was incised. After hemostasis with gentle pressure, the incision was closed with one or two sutures (5-0 silk/nylon ophthalmic suture on a taper TF needle or equivalent). The wound site was coveredwith a mixture of polymixin B, neomycin, and bacitracin ointment. After surgery, rats were allowed to recover in their cages until behavioral testing. Prior to surgery, rats were placed individually on an elevated wire mesh floor covered with a clearplastic cage top and allowed to acclimate. Baseline pain behavior was measured as follows: Withdrawal responses to mechanical stimulation were determined using von Frey filaments applied from underneath the cage through openings (12×12 mm in theplastic mesh floor to an area adjacent to the intended incision). Each von Frey filament (Target force of 0.008 g to 300 g) was applied once starting with 0.008 g filament and continuing until a withdrawal response occurred or 300 g force was reached. The median force producing a response, determined from three tests given over a 10-min period was considered the withdrawal threshold. Rats were tested for responses 15 minutes pre-surgery, 150 minutes after surgery, and 20 minutes after treatment. Oral treatments 1 and 2 were co-administered 180 minutes after surgery. The test article/vehicle administration and pain measurements were as per Table below. As illustrated by Table VI, SEQ ID NOs: 1 and 153 attenuate sensitization to von Frey mechanical stimuli after oral application. The response to the von Frey monofilament is in gram. Arrow up (1) indicates an increase in the pain threshold andarrow down (1) indicates a decrease in the threshold. Zero indicates no change. TABLE-US-00006 TABLE VI Oral administeration of SEQ ID NO: 1 and SEQ ID NO: 153 Withdrawal Response (g) Group Oral Pre- Post- Post- # Treatment 1 Treatment 2 Surgery Surgery Dose 1 0.9% Saline 0.9% Saline 26.0 . -. 3.90 3.9 . -. 0.27 3.7 . -. 0.52 (↓) 2 mL/kg 10 mL/kg 2 0.9% Saline Morphine sulfate 30.4 . -. 3.29 3.8 . -. 0.52 6.6 . -. 1.58 (↑) 2 mL/kg 3.7 mg/kg (1 mM) 3 Naloxone Morphine sulfate 28.5 . -. 4.53 3.7 . -. 0.39 3.5 . -. 0.24 (0) 2 mg/kg (1 mM) 3.7 mg/kg 4 ASAMorphine sulfate 21.9 . -. 2.13 4.3 . -. 0.41 5.5 . -. 0.80(↑) 1 mg/kg (1 mM) 3.7 mg/kg 5 Naloxone SEQ ID NO: 1 25.2 . -. 4.95 3.8 . -. 0.55 4.8 . -. 0.44 (↑) 2 mg/kg 100 mg/kg (0.2 mM) 6 ASA SEQ ID NO: 1 21.1 . -. 2.43 5.2 . -. 0.674.9 . -. 0.55 (0) 1 mg/kg 100 mg/kg 7 0.9% Saline SEQ ID NO: 1 25.9 . -. 3.44 3.7 . -. 0.23 5.1 . -. 1.00 (↑) 2 mL/kg 100 mg/kg 8 Naloxone SEQ ID NO: 153 29.3 . -. 4.00 4.5 . -. 0.55 4.7 . -. 0.45 (0) 2 mg/kg 100 mg/kg (0.2 mM) 9 ASA SEQ IDNO: 153 29.2 . -. 3.21 4.7 . -. 0.56 5.7 . -. 0.56 (↑) 1 mg/kg 100 mg/kg 10 0.9% Saline SEQ ID NO: 153 28.1 . -. 3.02 4.5 . -. 0.32 5.0 . -. 0.41 (0) 2 mL/kg 100 mg/kg As shown, the pain threshold is increased by the administration of Morphine (Group 2, pain sensitivity is reduced such that the rats can withstand up to 6.6 grams of pressure). Similarly, oral administration of SEQ ID NO: 1 and SEQ ID NO: 153(Groups 7 and 10, respectively) also increases the pain threshold (i.e., alleviates pain). For example in Group 7, when SEQ ID NO 1 was given orally after surgery it increased the pain threshold and consequently, the rats' pain tolerance went up from3.7 grams to 5.1 grams of von Frey filaments. Also, in Group 10, SEQ ID NO: 153 given orally after surgery and consequently, the rats' pain tolerance increased from 4.5 grams to 5.0 grams. Next, the mechanism of action of these peptides as binding agents of an opioid receptor was demonstrated with Naloxone--an antagonist of the opioid receptors. For example, in Group 3, when Naloxene is administered with Morphine, the effect ofMorphine is eliminated, i.e., Naloxene is an antagonist to Morphine and competes for the binding sites of the opioid receptor. When Naloxene was administered with SEQ ID NO: 153 (Group 8), the effects of SEQ ID NO: 153 were reduced (compare Group 8 toGroup 10) but unlike the case of Morphine (Group 3), not completely eliminated. Thus, SEQ ID NO: 153 binds to the opioid receptor more tightly than Morphine, but less tightly than Naloxene. When SEQ ID NO: 1 was administered with Naloxene (Group 5), itstill was able to alleviate pain (Compare Group 5 to Group 7). Thus, SEQ ID NO: 1 also binds the opioid receptor more tightly than Morphine, but still less tightly than Naloxene. In comparing the effects of asparin (ASA) to the peptides, rats in Group 4 were administered Morphine and Aspirin. The above table illustrates that aspirin reduced the effects of Morphine. Thus, aspirin is a competitive inhibitor and anantagonist or partial antagonist of Morphine. (Hence the present invention contemplates the use of aspirin to reduce the effects of Morphine i.e., in Morphine overdose.) Similar analysis was then conducted on the effects of aspirin on the therapeutic effects of SEQ ID NOS: 1 and 153. For example, Groups 6 rats were administered aspirin and SEQ ID NO: 1. These rats experience a reduced effect of SEQ ID NO: 1(4.9 grams in Group 6 as compared to 5.1 grams in Group 7). Therefore, ASA is a partial antagonist of SEQ ID NO 1 and binds the same opioid or aspirin receptor. On the other hand, Group 9 rats were administered aspirin and SEQ ID NO: 153. These rats experienced an improved effect of SEQ ID NO: 153 (5.7 grams in Group 9 as compared to 5.0 grams in Group 10). Therefore, ASA is a partial agonist or anagonist of SEQ ID NO: 153. Example 12 Groups of 10 male rats were weighed, color coded, and rectal temperatures were taken and recorded. Food was removed with water available ad libitum. Two groups of 10 rats each were injected subcutaneously with 5 mL of the 15% yeast suspensioninto the central dorsal region and one group of 10 rats was injected with saline. Twenty-three hours (. -.15 minutes) after injection, body weights and rectal temperatures were taken and recorded. Twenty-four hours (. -.15 minutes) after yeastinjection, the test article or vehicle were administered by subcutaneous injection to the 2 groups treated with yeast and the vehicle group was treated with 50 mg/kg of SEQ ID NO: 1 to check for pyretic activity. Rectal temperatures were taken andrecorded one hour (5. -.minutes) following test or control article administration (Chattopadhyay, D., Arunachalam, G., Ghosh, L., Rajendran, K., Mandal, A. B., Bhattacharya, S. K. Antipyretic activity of Alstonia macrophylla Wall ex. A. D C: Anethnomedicine of Andaman Islands. J. Pharm. Pharmaceut. Sci. 8 (3): 558-564, 2005; Kido, H., Murakami, N., Ito, A., Kimura, K., Kodera, N., Doi, T., and Naruse, T. Anti-inflammatory, analgesic and antipyretic effects ofd-2-[4-(3-Methyl-2-thienyl)phenyl]propionic acid (M-5011), a new non-steroidal antiinflammatory drug in rats and guinea pigs. Jpn. J. Pharmacol. 76: 75-86, 1998). TABLE-US-00007 TABLE VII Antipyretic effect of SEQ ID NO: 1. Sub- Rectal Temperature (° C.) Pre- cutaneous 1 hour Treat- Adminis- Pre-Test Post-Test ment tration Predose Article Article Saline SEQ ID NO: 1 38.5 . -. 0.07 37.5 . -. 0.05 36.9 . -. 0.11 5 ml/kg 50 mg/kg Yeast SEQ ID NO: 1 38.3 . -. 0.07 39.2 . -. 0.07 38.6 . -. 0.13 5 ml/kg 50 mg/kg Yeast SEQ ID NO: 1 38.2 . -. 0.09 39.2 . -. 0.10 38.7 . -. 0.18 5 ml/kg 100 mg/kg The above data illustrates that SEQ ID NO: 1 reduces core temperature and fever in rats. TABLE-US-00008 TABLE VIII Sequence listings. SEQ ID NO Sequence 1 FLPS 2 FLPSEFGVDVDR 3 KRFLPSEFGVDVDR 4 KRFFPSEFGLDVDR 5 KRFLPSEFGFDVDH 6 KRFFPSEFGNDVDK 7 KRFFPSEFGTDVDR 8 KRFLPSEFGMDPPR 9 KRFLPSEFGMDPAL 10 RRFLPSEFGLDPDH 11 KRFLPSEFGMDPDI 12KRFFPSEFGNDVDR 13 KKFYPSEFGNDVDR 14 VKRFFPSEFGLDVDR 15 YGGFL 16 YGGFM 17 YGGFLRKYPK 18 YGGPLRKYP 19 YGGFMTSEKSQTPLVTLFKNAIIKNAYKKGE 20 YGGFMTSEKSQTPLVT 21 YGGFLRRIRPKLKWDNQ 22 YGGFLRRQFKVVT 23 YPTF 24 YPFF 25 Tyr-D-Ala-Gly-N-Methyl-Phe-Gly-ol- 26Tyr-D-Pen-Gly-Phe-D-Pen 27 Tyr-D-Pen-Gly-D-Chloro-Phe-D-Pen 28 Tyr-D-Pen-Gly-Pen-Pen 29 Tyr-D-Ser-Gly-Phe-Leu-Thr 30 Tyr-D-Ala-Gly-Phe-D-Leu 31 Tyr-Gly-Gly-Phe-Met-Arg-Phe 32 D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr- 33 Ac-Arg-Tyr-Arg-Ile-Lys 34Tyr-D-Arg-Phe-Lys 35 Tyr-D-Ala-Gly-N-Methyl-Phe-Gly-ol 36 Tyr-D-Ala-Gly-Phe-D-Leu-D-Cys 37 Tyr-D-Ala-Phe-Glu-Val-Val-Pro Gly-amide 38 Tyr-D-Ala-Phe-Asp-Val-Val-Gly 39 Tyr-Pro-Methyl-Phe-D-Pro 40 N,N-diallyl-Tyr-Aib-Aib-Phe-Leu 41 YPFP 42FGGFTGARKSARKLANQ 43 TEPGLEEVGEIEGQKQLQ 44 AGEGLNSQFWSLAAPQRF 45 SQAFLFQPQRF 46 RPKPQQFFGLM 47 YPFVEPIP 48 YPFPGPI 49 DAEFRHDSGYEVHHQKLVFFAEDVGSNKGAIIGLMVGGVVIA 50 NPFLPS 51 NPYLPS 52 NPWLPS 53 NPHLPS 54 DPFLPS 55 DPYLPS 56 DPWLPS 57 DPHLPS 58 FLPPPPSS59 YLPPPPSS 60 WLPPPPSS 61 HLPPPPSS 62 GIPYTY 63 SIPYTY 64 TIPYTY 65 GVPYTY 66 GIPFTY 67 NIPFTY 68 GIPFTF 69 GIPHTY 70 YTIKAVDD 71 YTINAVDD 72 YTIEAVDD 73 YTINSVDD 74 YTIRAAND 75 YTIKTIDD 76 FTIKAAND 77 FTIKAVDD 78 SFGVEASELYPDVKYT 79 SWGLEASELYPDVKYT80 SFGVEATALYPDVKYT 81 HAVFVNG 82 HCVFVKG 83 HSVFVNG 84 HSAFVKG 85 HAAFVRG 86 HAGYIRG 87 HTAFVKG 88 HSSYVKG 89 90 DFTSFTIDPSFG 91 CFAGLFLFVPCLGGCH 92 HCGGLCPVFLFLGAFC 93 GAFYAAFC 94 GFSPDITFSTFD 95 TLFYGAFC 96 PLSYGAFF 97 PLSYGGFY 98 GAFYGAFM 99 FFAGYFLP100 CFGGYYLP 101 CFAAYFAG 102 CFAGYFLT 103 FFAGYSLP 104 YFGGYSLP 105 MFAGYFAG 106 YFAGYALP 107 WFADFFLP 108 PLFYGAFF 109 PLYYGGFC 110 TGYIGKFLV 111 TGYIGKFIV 112 TGYIGKFVA 113 TGYIGKYIV 114 TGYIGKYLV 115 TGYIGRHV 116 TGYLGRHV 117 TGYIGKRIV 118 TGFIGKRIV119 VLFKGIYGT 120 VIFKGIYGT 121 AVFKGIYGT 122 VIYKGIYGT 123 VLYKGIYGT 124 VHRGIYGT 125 VHRGLYGT 126 TYKVDPYLESAEVGFS 127 TYKVDPYLESAELGWS 128 TYKVDPYLATAEVGFS 129 TYKVDPYLESAEVGFS 130 TYKVDPYLESAELGWS 131 TYKVDPYLATAEVGFS 132 KIYLIK 133 KIYLVK 134 RIYLIK 135 RIYLVK 136 KILYIK 137 KVLYIK 138 KVLYIR139 IKKEWL 140 IKNEWL 141 TKKEWL 142 LKEWI 143 IKDEWL 144 IKGEWL 145 ILEEWK 146 LWEKKI 147 LWENKI 148 LWEKKT 149 IWEKL 150 LWEDKI 151 LWEGKI 152 KWEELI 153 SPLF 154 RDVDVGFESPLFRK 155 PFPY 156 SPLFPN 157 SPLYPN 158 SPLWPN 159 SPLHPN 160 SPLFPD 161 SPLYPD162 SPLWPD 163 SPLHPD 164 SSPPPPLF 165 SSPPPPLY 166 SSPPPPLW 167 SSPPPPLH 168 GTYPIG 169 YTYPIS 170 YTYPIT 171 YTYPVG 172 YTFPIG 173 YTFPIN 174 FTFPIG 175 YTHPIG 176 DDVAKITY 177 DDVANITY 178 DDVAEITY 179 DDVSNITY 180 DNAARITY 181 DDITKITY 182 DNAAKITF183 GNVFVAH 184 GKVFVCH 185 GNVFVSH 186 GKVFASH 187 GVFAAH 188 GRIYGAH 189 GKVFATH 190 GKVYSSH 191 GKVYSSH 192 CFAYFAG 193 194 195 196 197 PLFYGAFF 198 PLYYGGFC 199 GAFYAAFC 200 201 202 203 204 PLAYGAFY 205 PLFFDAFW 206 FFAGYFPL 207 208 VLFKGIYGT 209VIFKGIYGT 210 AVFKGIYTG 211 VIYKGIYGT 212 VLYKGIYGT 213 VHRGIYGT 214 VHRGLYGT 215 VIRKGIYGT 216 VIRKGIFGT 217 TGYIGKFLV 218 TGYIGKFIV 219 TGYIGKFVA 220 TGYIGKYIV 221 TGYIGKYLV 222 TGYIGRHV 223 TGYLGRHV 224 KILYIK 225 KVLYIK 226 KILYIR 227 KVLYIR 228KIYLIR 229 KIYLVK 230 RIYLVK 231 LWEKKI 232 LWENKI 233 LWEKKT 234 IWEKL 235 LWEDKI 236 LWEGKI 237 KWEELI 238 IKKEWL 239 IKNEWL 240 TKKEL 241 LKEKL 242 IKDEWL 243 IKGEWL 244 ILEEWK 245 MDKKSRVLIVGGTGFIGKRIVKASLALGHPTYVLFRPEALSYIDKVQMLISFKQLGAKLLEASLDDHQGLVDVVKQVDVVISAVSGGLVRHH ILDQLKLVEAIKEAGNIKR EFGMDPDVVEDPLEPGNITFIDK RKVRRAIEAATIPYTYVSSNMFAGFFAGSLAQLQDAPRMMPARDKV LIYGDGNVKGVYVDEDDAGIYIVKSIDDPRTLNKTVYIRPPMNILS QKEVVEIWERLSGLSLEKIYVSEDQLLNMKDKSYVEKMARCHLYHF FIKGDLYNFEIGPNATEGTKLYPEVKYTTMDSYM ERYL 246 MGESKRTEKTRVLVVGATGYIGKRIVRACLAEGHETYVLQRPEIGL EIEKVQLFLSFKKLGARIVEGSFSDHQSLVSAVKLVDVVVSAMSGV HFRSHNILVQLKLVEAIKEAGNVKR EFGMDPPRMGHALPPGR ETFDQKMERQAIEAAGIPYTYVVGACFAAYFAGNLSQMVTLLPPKEKVNIYGDGNVKVVFADEDDIAKYTAKTLNDPRTLNKTVNIRPPDNV LTQLELVQIWEKLTGKELEKTNLAAQDFLANIEQMEIPHQAGIGHF YHIFYEGCLTDHEVGEDEEASSLYPDVKYKRMDDYLRMFL 247 MATEKSKILVIGGTGYIGKFLVEASAKAGHSTFALVREATLSDPVK GKTVQSFKDLGVTILHGDLNDHESLVKAIKQVDVVISTVGSMQILD QTKIISAIKEAGNVKREFGVDVDRTSAVEPAKSAFAGKIQIR RTIEAEGIPYTYAVTGCFGGYYLPTLVQFEPGLTSPPRDKVTILGD GNAKAVINKEEDIAAYTIKAVDDPRTLNKILYIKPSNNTLSMNEIV TLWEKKIGKSLEKTHLPEEQLLKSIQESPIPINVVLSINHAVFVNG DTNISIEPSFGVEASELYPDVKYTSVDEYLSYFA 248 YGGFLRRQFKVVT 249KYPKRSSEVAGEGDGDSMGHEDLYKRYGGFLRRIRPKLKWDNQKRY GGFLRRQFKVVTRSQEDPNAYSGELFDA 250 MAWQGLVLAACLLMFPSTTADCLSRCSLCAVKTQDGPKPINPLICS LQCQAALLPSEEWERCQSFSFFTPSTLGLNDKEDLGSKSVGEGPYS ELAKLSGSFLKELEKSK ISTKENTLSKSLEEKLRGLSDGFRE GAESELMRDAQLNDGAMETGTLYLAEEDPKEQVKRKR SSEVAGEGDGDSMGHEDLYKR 251 ttt ctg ccc tca 252 ttt ctg ccc tca gaa ttt gga gta gac gta gac aga 253 MVKKIANDVSNKLFPLPKGFGDFVGIEDHIKAIKSILCLESKEARI MVGIWGQSGIGKSTIGRALFSQLSSQFHHRAFITYKSTSGSDVSGM KLSWEKELLSEILGQKDIKIDHFGVVEQRLKHKKVLILLDDVDNLEFLKTLVGKAEWFGSGSRIIVITQDKQLLKAHEIDLVYEVELPSQGL ALKMISQYAFGKDSPPDDFKELAFEVAELVGSLPLGLSVLGSSLKG RDKDEWVKMMPRLRNDSDDKIEETLRVGYDRLNKKNRDNVKELLED DVGLTMLADKSLIRITPDGDIEMHNLLEKLGREIDRAKSKGNPAKR QFLTNFEDIQEVVTEKTGTETVLGIRVPPTVLFSTRPLLVINEESFKGMQIGLWSKIDLPQGLVYLPLKLKLLKWNYCPLKSLPSTFKAEYL VNLIMKYSKLEKLWEGTLPLGSLKKMDLGCSNNLKEIPDLSLAINL EELNLSKCESLVTLPSSIQNAIKLRTLYCSGVLLIDLKSLEGMCNL EYLSVDWSSMEGTQGLIYLPRKLKRLWWDYCPVKRLPSNFKAEYLV ELRMENSDLEKLWDGTQPLGSLKEMYLHGSKYLKEIPDLSLAINLERLYLFGCESLVTLPSSIQNATKLINLDMRDCKKLESFPTDLNLESL EYLNLTGCPNLRNFPAIKMGCSYFEILQDRNEIEVEDCFWNKNLPA GLDYLDCLMRCMPCEFRPEYLTFLDVSGCKHEKLWEGIQIHALLDG YELAGHLDGSIETPAPTLTTNNVVSANPQYTLWKRQDRLIFSALIG AISPPVQPLVSRATKASQIWKTLTNTYAKSSYDHIKQLRTQIKQLKKGTKTIDEYVLSHTTLLDQLAILGKPMEHEEQVERILEGLPEDYKT VVDQIEGKDNTPSITEIHERLINHEAKLLSTAALSSSSLPMSANVA QQRHHNNNRNNNQNKNRTQGNTYTNNWQPSANNKSGQRPFKPYLGK CQICNVQGHSARRCPQLQAMQPSSSSSASTFTPWQPRANLAMGAPY TANNWLLDSGATHHITSDLNALALHQPYNGDDVMIADGTSLKITKTGSTFLPSNARDLTLNKVLYVPDIQKNLVSVYRLCNTNQVSVEFFPA SFQVKDLNTGTLLLQGRTKDELYEWPVTNPKATALFTTPSPKTTLS SWHSRLGHPSSSILNTLISKFSLPVSVSASNKLACSDCFINKSHKL PFSISSIKSTSPLEYIFSDVWMSPILSPDNYKYYLQKSQVKSTFIA FKALVENRFQAKIRTLYSDNGGEFIALREFLVSNGISHLTSPPHTPEHNGLSERKHRHIVETGLTLLTQASVPREYWPYAFAAAVYLINRMP TPVLSMESPFQKLFGSKPNYERLRVFGCLCFPWLRPYTHNKLEERS RRCVFLGYSTQTAYLCFDVEHKRLYTSRHVVFDEASFPFSNLTSQN SLPTVTFEQSSSPLVTPILSSSSVLPSCLSSPCTVLHQQQPPVTTP NSPHSSQPTTSPAPLSPHRSTTMDFQVPQPTAPNENGPEPEAQSPPIGPLSNPTHEAFIGPLPNPNRNPTNEIEPTPAPHPKPVKPTTTTTT PNRTTVSDASHQPTAPQQNQHNMKTRAKNNIKKPNTKFSLTATLPN RSPSEPTNVTQALKDKKWRFAMSDEFDAQQRNHTWDLVPHESQLLV GCKWVFKLKYLPNGAIDKYKARLVAKGFNQQYGVDYAETFSPVIKS TTIRLVLDVAVKKDWEIKQLDVNNAFLQGTLTEEVYMAQPPGFIDKDRPTHVCRLRKAIYGLKQAPRAWYMELKQHLFNIGFVNSLSDASLF IYWSDKSSIDAVLTSLAERFSIKDPTDLHYFLGIEATRTKQGLHLM QRKYIKDLLAKHNMADAKPVLTPLPTSPKLTLHGGTKLNDASEYRS VVGSLQYLAFTRPDIAYAVNRLSQLMPQPTEDHWQAAKRVLRYLAG TSTHDWAGDSDDYVSTNAYVIYLGKNPISWSSKKQRGVARSSTESEYRAVANAASEVKWLCSLLSKLHIRLPIRPSIFCDNIGATYLCANPV FHSRMKHIAIDYHFVRNMIQSGALRVSHVSTRDQLADALTKPLSRA HFQSARFKIGVRQLPPS 254 MSTSSLRRQMKNIVHNYSEAIEIKVREATSNDPWGPSSSLMSEIAD LTYNVVAFSEIMSMIWKRLNDHGKNWRHVYKAMTLMEYLIKTGSERVSQQCKENMYAVQTLKDFQYVDRDGKDQGVNVREKAKQLVALLRDE DRLREERAHALKTKEKLAQTATASSAAVGSGPPPEAEQAWPQSSGE EELQLQLALAMSKEEADQPPSCGPEDDVQLQLALSLSREEHDKEER IRRGDDLRLQMAIEESKRETGGKEESSLMDLADVFTTPAPPQASDP WGGPASVPTAVPVAAAASDPWGAPAVPPAADPWGGAAPTPASGDPWRPAAPTGPSVDPWGGTPAPAAGEGPTSDPWGSADGGAPVSGPPSSD PWAPAPAFSDPWGGSPAKPSSNGTAVGGFDTEPDEFSDFDRLRTAL PTSGSSTGELELLAGEVPARSPGAFDMSGVGGSLAESVGSPPPAAT PTPTPPTRKTPESFLGPNAALVDLDSLVSRPGPTPPGAKASNP GAPATGPSVTNPFQPAPPATLTLNQLRLSPVPPVPGAPPTYISPLGGGPGLPPMMPPGPPAPNTNPFLL 255 MEPPLPVGAQPLATVEGMEMKGPLREPCALTLAQRNGQYELIIQLH EKEQHVQDIIPINSHFRCVQEAEETLLIDIASNSGCKIRVQGDWIR ERRFEIPDEEHCLKFLSAVLAAQKAQSQLLVPEQKDSSSWYQKLDT KDKPSVFSGLLGFEDNFSSMNLDKKINSQNQPTGIHREPPPPPFSVNKMLPREKEASNKEQPKVTNTMRKLFVPNTQSGQREGLIKHILAKR EKEYVNIQTFRFFVGTWNVNGQSPDSGLEPWLNCDPNPPDIYCIGF QELDLSTEAFFYFESVKEQEWSMAVERGLHSKAKYKKVQLVRLVGM MLLIFARKDQCRYIRDIATETVGTGIMGKMGNKGGVAVRFVFHNTT FCIVNSHLAAHVEDFERRNQDYKDICARMSFVVPNQTLPQLNIMKHEVVIWGDLNYRLCMPDANEVKSLINKKDLQRLLKFDQLNIQRTQKK AFVDFNEGEIKFIPTYKYDSKTDRWDSSGKCRVPAWCDRILWRGTN VNQLNYRSHMELKTSDHKPVSALFHIGVKVVDERRYRKVFEDSVRI MDRMEND LELSRREFVFENVKFRQLQKEKFQISNNGQVPCHF SFIPKLNDSQYCKPWLRAEPFEGYLEPNETVDISLDVYVSKDSVTILNSGEDKIEDILVLHLDRGKDYFLTISGNYLPSCFGTSLEALCRMK RPIREVPVTKLIDLEEDSFLEKEKSLLQMVPLDEGASERPLQVPKE IWLLVDHLFKYACHQEDLFQTPGMQEELQQIIDCLDTSIPETIPGS NHSVAEALLIFLEALPEPVICYELYQRCLDSAYDPRICRQVISQLP RCHRNVFRYLMAFLRELLKFSEYNSVNANMIATLFTSLLLRPPPNLMARQTPSDRQRAIQFLLGFLLGSEED 256 MSESGNTTSMPGCGRMCALRSTWSKRAFLVACKDGALTSDGRCPQY GCGALVSITKGVQQPKKTASAKVVKCLCWVQPARWCEKHSKGPASP NGSVTTKRSNSARAAPAPLPYKKQTCDVVVTVGPLELVYPALVSEE LPTPVAATPTKVEEVPIPELPLWLAPAWMVEQPYAATPEVLCLTQREEFALLKKRLTRKGKLLQRRATHARFEARAALARVRAATQRKVEEV TALVIKGRRILAAHQLLRELEEVAPLSQAQEQLVASSCAAAAARQE ECASFLRRAKAWRKSISATPPVAATAVASKVVSATMPWAHLGLSLG GLLAVPTLDGTLGAKQWNAKTIATWVLKPVVSCVQSVHAKVRDWLH SQPEVGVTNTKVPLVLPEVCLGVLSPPSLSEEIVDNPQETSQSGIWHPEMGVRNIYVFHDDSWETSPEEDENYTYTFSRQCGIPYLLVEGRG AEERKNTILGWDFSLHNDGFEFLPSPEEGYTKELVTPVALEEEDKY STASSCGFFSLDDVSSAITIQCPGLLSADADVHFFDGPGYRCSSRP RDFRPPVVRGCDYESRVKASIQRKIENPLQERFITVLREKRKKNKK KEFHSFSACFAFKRKQIQWPPTPNEMVNEWEEYCIAQAWLPFEVVVTDEIEDVTPLYPGGRDYNCNSQLLFPLAPLSTVYCDDSCFHPNDGW TTDGNGKHFRLSPQFVLPDVPIPIVHRVTRQLPQFLYDLGIGDLTC NSGYQAENLQEEIQERMEDRSEEKPVPSLDTLISKLSKRSTKVKGA GENRYADRHSLTEKAIFHQPGALSRMRSGKEKTIVAANHNSDQISV RMAECGKPVFTPLPRMSDEMLRKFLEKGLGSTSTVALDIGIQSHIPQGMPTVAFVNVMDTRIEDPLYSSLCGSYIDLGRDRAKTLCLPLVNF PMSKLAEDVDDVLNGLMLCTHFQDSTKFGVGKPAFQYGTLEFQEFK PSAYSDFSRVRDNWDAIAKQQNTPNDRILAGFSVLGAVSQAYNQAL PVFKSVELVAPPKRKPVVATFQNPTTLGRSNTTRSFRMPTMDLPRS TGRDAPIPIVHRRNNNDVHFDEATPARFSTCDSGLVADTTLAFAKMYQCKKDAKAGHVLATIDIQECVFEDNRRVALDWLAHGLASFKYDLQ LTVDSNPFVGVTLGITVDAFDRLLPQISDEVIAVPLAFQLPTYLFP ISKKGTFTQTIDFAAIAGYNFFPHVAAFGRPKIIVYIVSDNDLPAS DTWMCLVELHMTRLESSTLACSPTLVLPQAFGGDLPLDLWRGPYTF PLGGGTKRLSTSLDIGTSTTTVSGWRTVSPAAYALFLQGHGGSLVGEVVHTGSAAVSCALHLCISFGGAPPTLEEALVFPGFRLPSGEGKFH IKVQTPYGRLSTLTPDCALYVYLAGGPIAVAPMSVPYQFCIHLERL VDDGAPPRTIGLIREFNWATINNFKSDDITFAIPARLSDLVLTCGD VTMSTNPLALLIGSCGFFRGNLTVVLEWATFLKAGDKEGTVQLTTC RGMINNVKGVRNAIQKKVVNLSLVGSVSRYLNVGDFTGFAQSGGQVGYDEIFLEFSTNKAKQIRYLNINVELDENFELYGRTIIPLKNTAPA FASTSSAPNES 257 KFLPS 258 FLPSI 259 RFLPS 260 FLPSE 261 SFLK 262 WERC 263 FSFFTP 264 FFNP 265 FPST 266 SFLG 267 YSEL 268 SYLG 269 SWLG 270 FFTPS 271 SFLSFFTPS 272 NPFQP 273 MSFLK 274 FLPPPS 275 FLPPS 276MFPST 277 FLPPPPPPS 278 FLPPPPPS 279 FGGFIM 280 KLFS 281 CREW 282 PTFFSF 283 PNFF 284 TSPF 285 GLFS 286 LESY 287 GLYS 288 GLWS 289 SPTFF 290 SPTFFSLFS 291 PQFPN 292 KLFSM 293 SPPPPLF 294 SPPLF 295 TSPFM 296 SPPPPPPPLF 297 SPPPPPPLF 298 MIFGGF 299MAWQGLVLAACLLMFPSTTADCLSRCSLCAVKTQDGPKPINPLICS LQCQAALLPSEEWERCQSFLSFFTPSTLGLNDKEDLGSKSVGEGPY SELAKLSGSFLKELEKSKFLPSISTKENTLSKSLEEKLRGLSDGFR EGAESELMRDAQLNDGAMETGTLYLAEEDPKEQVKR 300 MARFLTLCTWLLLLGPGLLATVRAECSQDCATCSYRLVRPADINFLACVMECEGKLPSLKIWETCKELLQLSKPELPQDGTSTLRENSKPEE SHLLAKRY 301 MARFLTLCTWLLLLGPGLLATVRAECSQDCATCSYRLVRPADINFL ACVMECEGKLPSLKIWETCKELLQLSKPELPQDGTSTLRENSKPEE SHLLAKRYGGFMKRYGGFMKKMDELYPMEPEEEANGSEILAKRYGG FMKKDAEEDDSLANSSDLLKELLETGDNRERSHHQDGSDNEEEVSKRYGGFMRGLKRSPQLEDEAKELQKRYGGFMRRVGRPEWWMDYQKRY GGFLKRFAEALPSDEEGESYSKEVPEMEKRYGGFMRF 302 MPRSCCSRSGALLLALLLQASMEVRGWCLESSQCQDLTTESNLLEC IRACKPDLSAETPMFPGNGDEQPLTENPRKYVMGHFRWDRFGRRNS SSSGSSGAGQKREDVSAGEDCGPLPEGGPEPRSDGAKPGPREGKRS YSMEHFRWGKPVGKKRRPVKVYPNGAEDESAEAFPLEFKRELTGQRLREGDGPDGPADDGAGAQADLEHSLLVAAEKKDEGPYRMEHFRWGS PPKDKRYGGFMTSEKSQTPLVTLFKNAIIK NAYKKGE 303 MPRSCCSRSGALLLALLLQASMEVRGWCLESSQCQDLTTESNLLEC IRACKPDLSAETPMFPGNGDEQPLTENPRKYVMGHFRWDRFGRRNS SSSGSSGAGQKREDVSAGEDCGPLPEGGPEPRSDGAKPGPREGKRSYSMEHFRWGKPVGKKRRPVKVYPNGAEDESAEAFPLEFKRELTGQR LREGDGPDGPADDGAGAQADLEHSLLVAAEKKDEGPYRMEHFRWGS PPKDKR 304 FLPSPLF 305 FLPSSPLF 306 PFLP 307 SLFP 308 FPSA 309 310 AFLP 311 TLPF 312 PPLF 313 FPSP 314 FLVS 315 PLFP 316 FLFS 317 LFSF 318 MFTS 319 PSLF 320PSSF 321 FTPS 322 FLSF 323 LPSF 324 FKPS 325 FLSP 326 FPLS 327 FPSL 328 FSPL 329 FSLP 330 LFPS 331 LFSP 332 LPFS 333 LSPF 334 LSFP 335 PFLS 336 PFSL 337 PLSF 338 PLFS 339 PSFL 340 SFLP 341 SFPL 342 SPFL 343 SLPF 344 FLP 345 FPL 346 PLF 347 LPF 348 LFP349 PFL > SEQUENCE LISTING < NUMBER OF SEQ ID NOS: 353 <2SEQ ID NO LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: eu Pro Ser SEQ ID NO 2 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2 Phe Leu Pro Ser Glu Phe Gly Val Asp Val Asp Arg <2SEQ ID NO 3 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3 Lys Arg Phe Leu Pro Ser Glu Phe Gly Val Asp Val Asp Arg <2SEQ ID NO 4<2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 4 Lys Arg Phe Phe Pro Ser Glu PheGly Leu Asp Val Asp Arg <2SEQ ID NO 5 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 5 Lys Arg Phe Leu Pro Ser Glu Phe Gly Phe Asp Val Asp His <2SEQ ID NO 6 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 6 Lys Arg Phe Phe Pro Ser Glu Phe Gly Asn Asp Val Asp Lys <2SEQ ID NO 7 <2LENGTH: 2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 7 Lys Arg Phe Phe Pro Ser Glu Phe Gly Thr Asp Val Asp Arg <2SEQ ID NO 8 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 8 Lys Arg Phe Leu Pro Ser Glu Phe Gly Met Asp Pro Pro Arg<2SEQ ID NO 9 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 9Lys Arg Phe Leu Pro Ser Glu Phe Gly Met Asp Pro Ala Leu <2SEQ ID NO 2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: Arg Phe Leu Pro Ser Glu Phe Gly Leu Asp Pro Asp His <2SEQ ID NO 2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Arg Phe Leu Pro Ser Glu Phe Gly Met Asp Pro Asp Ile <2SEQ ID NO 2LENGTH: 2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Arg Phe Phe Pro Ser Glu Phe Gly Asn Asp Val Asp Arg <2SEQ ID NO 2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Phe Tyr ProSer Glu Phe Gly Asn Asp Val Asp Arg <2SEQ ID NO 2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: Lys Arg Phe Phe Pro Ser Glu Phe Gly Leu Asp Val Asp Arg 2SEQ ID NO 2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Gly Phe Leu ;2SEQ ID NO 2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Gly Phe Met ;2SEQ ID NO 2LENGTH: 2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Gly Phe Leu Arg Lys Tyr Pro Lys <2SEQ ID NO 2LENGTH: 9 <2TYPE:PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Gly Pro Leu Arg Lys Tyr Pro ;2SEQ ID NO 2LENGTH: 3TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Gly Phe Met Thr Ser GluLys Ser Gln Thr Pro Leu Val Thr Phe Lys Asn Ala Ile Ile Lys Asn Ala Tyr Lys Lys Gly Glu 2 <2SEQ ID NO 2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2ly Gly Phe Met Thr Ser Glu Lys Ser Gln Thr Pro Leu Val Thr 2SEQ ID NO 2LENGTH: 2TYPE:PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2ly Gly Phe Leu Arg Arg Ile Arg Pro Lys Leu Lys Trp Asp Asn <2SEQ ID NO 22 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 22 TyrGly Gly Phe Leu Arg Arg Gln Phe Lys Val Val Thr <2SEQ ID NO 23 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 23 Tyr Pro Thr Phe SEQ ID NO 24 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 24 Tyr Pro Phe Phe SEQ ID NO 25 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Ala <22EATURE: <22AME/KEY: MOD_RES LOCATION: (4) OTHERINFORMATION: N-Methyl-Phe <4SEQUENCE: 25 Tyr Ala Gly Phe Gly ;2SEQ ID NO 26 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Pen <22EATURE: <22AME/KEY: MOD_RES LOCATION: (5) OTHERINFORMATION: D-Pen <4SEQUENCE: 26 Tyr Xaa Gly Phe Xaa ;2SEQ ID NO 27 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Pen <22EATURE: <22AME/KEY: MOD_RES LOCATION: (4) OTHERINFORMATION: D-Chloro-Phe <22EATURE: <22AME/KEY: MOD_RES LOCATION: (5) OTHER INFORMATION: D-Pen <4SEQUENCE: 27 Tyr Xaa Gly Phe Xaa ;2SEQ ID NO 28 <2LENGTH: 5 <2TYPE:PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHERINFORMATION: D-Pen <22EATURE: <22AME/KEY: MOD_RES LOCATION: (4)..(5) OTHER INFORMATION: Pen <4SEQUENCE: 28 Tyr Xaa Gly Xaa Xaa ;2SEQ ID NO 29 <2LENGTH: 6 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHERINFORMATION: D-Ser <4SEQUENCE: 29 Tyr Ser Gly Phe Leu Thr ;2SEQ ID NO 3LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Ala <22EATURE: <22AME/KEY: MOD_RES LOCATION: (5) OTHER INFORMATION: D-Leu <4SEQUENCE: 3la Gly Phe Leu ;2SEQ ID NO 3LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3ly Gly Phe Met Arg Phe ;2SEQ ID NO 32 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (223> OTHER INFORMATION: D-Phe <22EATURE: <22AME/KEY:MOD_RES LOCATION: (4) OTHER INFORMATION: D-Trp <22EATURE: <22AME/KEY: MOD_RES LOCATION: (5) OTHER INFORMATION: Orn <22EATURE: <22AME/KEY: MOD_RES LOCATION: (7) OTHER INFORMATION: Pen <4SEQUENCE: 32 Phe Cys Tyr Trp Xaa Thr Xaa Thr ;2SEQ ID NO 33 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 33 Arg Tyr Arg Ile Lys ;2SEQ ID NO 34 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Arg <4SEQUENCE: 34 Tyr Arg Phe Lys SEQ ID NO 35 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Ala <22EATURE: <22AME/KEY: MOD_RES LOCATION: (4) OTHER INFORMATION: N-Methyl-Phe <4SEQUENCE: 35 Tyr Ala Gly Phe Gly ;2SEQ ID NO 36 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Ala <22EATURE: <22AME/KEY: MOD_RES LOCATION: (5) OTHER INFORMATION: D-Leu <22EATURE: <22AME/KEY: MOD_RES LOCATION: (6) OTHER INFORMATION: D-Cys <4SEQUENCE: 36 Tyr Ala Gly Phe Leu Cys ;2SEQ ID NO 37 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Ala <22EATURE: OTHER INFORMATION:C-term amidated <4SEQUENCE: 37 Tyr Ala Phe Glu Val Val Pro Gly ;2SEQ ID NO 38 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2) OTHER INFORMATION: D-Ala <4SEQUENCE: 38 Tyr Ala Phe Asp Val Val Gly ;2SEQ ID NO 39 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (3) OTHER INFORMATION: Methyl-Phe <22EATURE: <22AME/KEY: MOD_RES LOCATION: (4) OTHER INFORMATION: D-Pro <4SEQUENCE: 39 Tyr Pro Phe Pro SEQ ID NO 4LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <22EATURE: <22AME/KEY: MOD_RES LOCATION: (223> OTHER INFORMATION: N,N-diallyl-Tyr <22EATURE: <22AME/KEY: MOD_RES LOCATION: (2)..(3) OTHER INFORMATION: Aib <4SEQUENCE: 4aa Xaa Phe Leu ;2SEQ ID NO 4LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 4ro Phe Pro SEQID NO 42 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 42 Phe Gly Gly Phe Thr GlyAla Arg Lys Ser Ala Arg Lys Leu Ala Asn <2SEQ ID NO 43 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 43 Thr Glu Pro Gly Leu Glu Glu Val Gly Glu Ile Glu Gly Gln Lys Gln Gln <2SEQ ID NO 44 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 44 Ala Gly Glu Gly Leu Asn Ser Gln Phe Trp Ser Leu Ala Ala Pro Gln Phe <2SEQ ID NO 45 <2LENGTH: 2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 45 Ser Gln Ala Phe Leu Phe Gln Pro Gln Arg Phe <2SEQ ID NO 46<2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 46 Arg Pro Lys Pro Gln Gln Phe PheGly Leu Met <2SEQ ID NO 47 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 47 Tyr Pro Phe Val Glu Pro Ile Pro ;2SEQ ID NO 48 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 48 Tyr Pro Phe Pro Gly Pro Ile ;2SEQ ID NO 49 <2LENGTH: 42 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Descriptionof Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 49 Asp Ala Glu Phe Arg His Asp Ser Gly Tyr Glu Val His His Gln Lys Val Phe Phe Ala Glu Asp Val Gly Ser Asn Lys Gly Ala Ile Ile 2 Gly Leu Met Val Gly Gly Val Val IleAla 35 4SEQ ID NO 5LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE:5ro Phe Leu Pro Ser ;2SEQ ID NO 5LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 5ro Tyr Leu Pro Ser ;2SEQ ID NO 52 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 52 Asn Pro Trp Leu Pro Ser ;2SEQ ID NO 53 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 53 Asn Pro His Leu Pro Ser ;2SEQ ID NO 54 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 54 Asp Pro Phe Leu Pro Ser ;2SEQ ID NO 55 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 55 Asp Pro Tyr Leu Pro Ser ;2SEQ ID NO 56 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 56 Asp Pro Trp Leu Pro Ser ;2SEQ ID NO 57 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 57 Asp Pro His Leu Pro Ser ;2SEQ ID NO 58 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 58 Phe Leu Pro Pro Pro Pro Ser Ser ;2SEQ ID NO 59 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 59 Tyr Leu Pro Pro Pro Pro Ser Ser ;2SEQ ID NO 6LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 6eu Pro Pro Pro Pro Ser Ser ;2SEQ ID NO 6LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 6eu Pro Pro Pro Pro Ser Ser ;2SEQ ID NO 62 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 62 Gly Ile Pro Tyr Thr Tyr ;2SEQ ID NO 63 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 63 Ser Ile Pro Tyr Thr Tyr ;2SEQ ID NO 64 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 64 Thr Ile Pro Tyr Thr Tyr ;2SEQ ID NO 65 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 65 Gly Val Pro Tyr Thr Tyr ;2SEQ ID NO 66 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 66 Gly Ile Pro Phe Thr Tyr ;2SEQID NO 67 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 67 Asn Ile Pro Phe Thr Tyr;2SEQ ID NO 68 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 68 GlyIle Pro Phe Thr Phe ;2SEQ ID NO 69 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 69 Gly Ile Pro His Thr Tyr ;2SEQ ID NO 7LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 7hr Ile Lys Ala Val Asp Asp ;2SEQ ID NO 7LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 7hr Ile Asn Ala Val Asp Asp ;2SEQ ID NO 72 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 72 Tyr Thr Ile Glu Ala Val Asp Asp ;2SEQ ID NO 73 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 73 Tyr Thr Ile Asn Ser Val Asp Asp ;2SEQ ID NO 74 <2LENGTH: 8 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 74 Tyr Thr Ile Arg Ala Ala Asn Asp ;2SEQ ID NO 75 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 75 Tyr Thr Ile Lys Thr Ile Asp Asp ;2SEQ ID NO 76 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 76 Phe Thr Ile Lys Ala Ala Asn Asp ;2SEQ ID NO 77 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 77 Phe Thr Ile Lys Ala Val Asp Asp ;2SEQ ID NO 78 <2LENGTH: 2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 78 Ser Phe Gly Val Glu Ala Ser Glu Leu Tyr Pro Asp Val Lys Tyr Thr 2SEQ ID NO 79 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 79 Ser Trp Gly Leu Glu Ala Ser Glu Leu Tyr ProAsp Val Lys Tyr Thr 2SEQ ID NO 8LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 8he Gly Val Glu Ala Thr Ala Leu Tyr Pro Asp Val Lys Tyr Thr 2SEQ ID NO 8LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 8la Val Phe Val Asn Gly ;2SEQ ID NO 82 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 82 His Cys Val Phe Val Lys Gly ;2SEQ ID NO 83 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 83 His Ser Val Phe Val Asn Gly ;2SEQ ID NO 84 <2LENGTH: 7 <2TYPE:PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 84 His Ser Ala Phe Val Lys Gly ;2SEQ ID NO 85 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 85 His Ala Ala Phe Val Arg Gly ;2SEQ ID NO 86 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 86 His Ala Gly Tyr IleArg Gly ;2SEQ ID NO 87 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE:87 His Thr Ala Phe Val Lys Gly ;2SEQ ID NO 88 <2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 88 His Ser Ser Tyr Val Lys Gly ;2SEQ ID NO 89 <4SEQUENCE: 89 ;2SEQ ID NO 9LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 9he Thr Ser Phe Thr Ile Asp Pro Ser Phe Gly <2SEQ ID NO 9LENGTH: 2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 9he Ala Gly Leu Phe Leu Phe Val Pro Cys Leu Gly Gly Cys His 2SEQ ID NO 92 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 92 His Cys Gly Gly Leu Cys Pro Val Phe Leu Phe Leu Gly Ala Phe Cys 2SEQ ID NO 93 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 93 Gly Ala Phe Tyr Ala Ala Phe Cys ;2SEQ ID NO 94 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 94 Gly Phe Ser Pro Asp Ile Thr Phe Ser Thr Phe Asp <2SEQ ID NO 95 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 95 Thr Leu Phe Tyr Gly Ala Phe Cys ;2SEQ ID NO 96 <2LENGTH: 8<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 96 Pro Leu Ser Tyr Gly Ala Phe Phe ;2SEQ IDNO 97 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 97 Pro Leu Ser Tyr Gly Gly PheTyr ;2SEQ ID NO 98 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 98Gly Ala Phe Tyr Gly Ala Phe Met ;2SEQ ID NO 99 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 99 Phe Phe Ala Gly Tyr Phe Leu Pro ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Gly Gly Tyr Tyr Leu Pro ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Ala Ala Tyr Phe Ala Gly ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Ala Gly Tyr Phe Leu Thr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Ala Gly Tyr Ser Leu Pro ;2SEQ ID NO ;2LENGTH: 8<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Gly Gly Tyr Ser Leu Pro ;2SEQ IDNO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Ala Gly Tyr PheAla Gly ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Phe Ala Gly Tyr Ala Leu Pro ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: Phe Ala Asp Phe Phe Leu Pro ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Leu Phe Tyr Gly Ala Phe Phe ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Leu Tyr Tyr Gly Gly Phe Cys ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr Ile Gly Lys Phe Leu Val ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr Ile Gly Lys Phe Ile Val ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr Ile Gly Lys Phe Val Ala ;2SEQ ID NO ;2LENGTH: 9<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr Ile Gly Lys Tyr Ile Val ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr IleGly Lys Tyr Leu Val ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: Gly Tyr Ile Gly Arg His Val ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr Leu Gly Arg His Val ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Tyr Ile Gly Lys Arg Ile Val ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Gly Phe Ile Gly Lys Arg Ile Val ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Leu Phe Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ile Phe Lys Gly Ile Tyr GlyThr ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Val Phe Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: Ile Tyr Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO ;2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Descriptionof Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Leu Tyr Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: His Arg Gly Ile Tyr Gly Thr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: His Arg Gly Leu Tyr Gly Thr ;2SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Tyr Lys Val Asp Pro Tyr Leu Glu Ser Ala Glu Val Gly Phe Ser 2SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Tyr Lys Val Asp Pro Tyr Leu Glu Ser Ala Glu Leu Gly Trp Ser 2SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Tyr Lys Val Asp Pro Tyr Leu Ala Thr Ala Glu Val Gly Phe Ser 2SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Tyr Lys Val Asp Pro Tyr Leu Glu Ser Ala Glu Val Gly Phe Ser 2SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Tyr Lys Val Asp Pro Tyr LeuGlu Ser Ala Glu Leu Gly Trp Ser 2SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: Tyr Lys Val Asp Pro Tyr Leu Ala Thr Ala Glu Val Gly Phe Ser 2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ile Tyr Leu Ile Lys ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ile Tyr Leu Val Lys ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ile Tyr Leu Ile Lys ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ile Tyr Leu Val Lys ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ile Leu Tyr Ile Lys ;2SEQID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Val Leu Tyr IleLys ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Val Leu Tyr Ile Arg ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: Lys Lys Glu Trp Leu ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: Lys Asn Glu Trp Leu ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Lys Glu Trp Leu ;2SEQ ID NO ;2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Asp Glu Trp Leu ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: Lys Gly Glu Trp Leu ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: Leu Glu Glu Trp Lys ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Lys Lys Ile ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Asn Lys Ile ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Lys Lys Thr ;2SEQ ID NO ;2LENGTH: 5 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Lys Leu ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Asp Lys Ile ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Gly Lys Ile ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Trp Glu Glu Leu Ile ;2SEQID NO ;2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu Phe SEQ ID NO ;2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asp Val Asp Val Gly Phe Glu Ser Pro Leu Phe Arg Lys <2SEQ ID NO ;2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: Phe Pro Tyr SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu Phe Pro Asn ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu Tyr Pro Asn ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu Trp Pro Asn ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide Ser Pro Leu His Pro Asn ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: Pro Leu Phe Pro Asp ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu Tyr Pro Asp ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu Trp Pro Asp ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Pro Leu His Pro Asp ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ser Pro Pro Pro Pro Leu Phe ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ser Pro Pro Pro Pro Leu Tyr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ser Pro Pro Pro Pro Leu Trp ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ser Pro Pro Pro Pro Leu His ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: Thr Tyr Pro Ile Gly ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: Thr Tyr Pro Ile Ser ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: Thr Tyr Pro Ile Thr ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Thr Tyr Pro Val Gly ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Thr Phe Pro Ile Gly ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Thr Phe Pro Ile Asn ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Thr Phe Pro Ile Gly ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Thr His Pro Ile Gly ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asp Val Ala Lys Ile Thr Tyr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asp Val Ala Asn Ile Thr Tyr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asp Val Ala Glu Ile Thr Tyr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asp Val Ser Asn Ile Thr Tyr ;2SEQ ID NO ;2LENGTH: 8<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asn Ala Ala Arg Ile Thr Tyr ;2SEQ IDNO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asp Ile Thr Lys IleThr Tyr ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asn Ala Ala Lys Ile Thr Phe ;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: Asn Val Phe Val Ala His ;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Val Phe Val Cys His ;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Asn Val Phe Val Ser His ;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Val Phe Ala Ser His ;2SEQ ID NO ;2LENGTH: 6 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Val Phe Ala Ala His ;2SEQ ID NO ;2LENGTH: 7<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Arg Ile Tyr Gly Ala His ;2SEQ ID NO;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Val Phe Ala Thr His;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Lys Val Tyr Ser Ser His ;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: Lys Val Tyr Ser Ser His ;2SEQ ID NO ;2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: <2SEQ ID NO ;4SEQUENCE: <2SEQ ID NO ;4SEQUENCE: <2SEQ ID NO ;4SEQUENCE: <2SEQ ID NO ;2LENGTH: 8<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Leu Phe Tyr Gly Ala Phe Phe ;2SEQ IDNO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Leu Tyr Tyr Gly GlyPhe Cys ;2SEQ ID NO ;2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: Ala Phe Tyr Ala Ala Phe Cys ;2SEQ ID NO 24SEQUENCE: 2<2SEQ ID NO 24SEQUENCE: 2<2SEQ ID NO 24SEQUENCE: 2<2SEQ ID NO 24SEQUENCE: 2<2SEQ ID NO 22LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 2Leu Ala Tyr Gly Ala Phe Tyr ;2SEQ ID NO 22LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 2Leu Phe Phe Asp Ala Phe Trp ;2SEQ ID NO 22LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Phe Ala Gly Tyr Phe Pro Leu ;2SEQ ID NO 24SEQUENCE: 2<2SEQ ID NO 22LENGTH: 9 <2TYPE:PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Leu Phe Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Ile Phe Lys Gly Ile Tyr GlyThr ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE:2Val Phe Lys Gly Ile Tyr Thr Gly ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 2Ile Tyr Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Descriptionof Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Leu Tyr Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO 22LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2His Arg Gly Ile Tyr Gly Thr ;2SEQ ID NO 22LENGTH: 8 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2 Val His Arg Gly Leu Tyr Gly Thr ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 2Ile Arg Lys Gly Ile Tyr Gly Thr ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Descriptionof Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Ile Arg Lys Gly Ile Phe Gly Thr ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Gly Tyr Ile Gly Lys Phe Leu Val ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Gly Tyr Ile Gly Lys Phe Ile Val ;2SEQ ID NO 22LENGTH: 9<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 2Gly Tyr Ile Gly Lys Phe Val Ala ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 22ly Tyr IleGly Lys Tyr Ile Val ;2SEQ ID NO 22LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 22ly Tyr Ile Gly Lys Tyr Leu Val ;2SEQ ID NO 222 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 222 Thr Gly Tyr Ile Gly Arg His Val ;2SEQ ID NO 223 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 223 Thr Gly Tyr Leu Gly Arg His Val ;2SEQ ID NO 224 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 224 Lys Ile Leu Tyr Ile Lys ;2SEQ ID NO 225 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 225 Lys Val Leu Tyr Ile Lys ;2SEQ ID NO 226 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 226 Lys Ile Leu Tyr Ile Arg ;2SEQ ID NO 227 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 227 Lys Val Leu Tyr Ile Arg ;2SEQID NO 228 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 228 Lys Ile Tyr Leu IleArg ;2SEQ ID NO 229 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE:229 Lys Ile Tyr Leu Val Lys ;2SEQ ID NO 23LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 23le Tyr Leu Val Lys ;2SEQ ID NO 23LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 23rp Glu Lys Lys Ile ;2SEQ ID NO 232 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 232 Leu Trp Glu Asn Lys Ile ;2SEQ ID NO 233 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 233 Leu Trp Glu Lys Lys Thr ;2SEQ ID NO 234 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 234 Ile Trp Glu Lys Leu ;2SEQ ID NO 235 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 235 Leu Trp Glu Asp Lys Ile ;2SEQ ID NO 236 <2LENGTH: 6 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 236 Leu Trp Glu Gly Lys Ile ;2SEQ ID NO 237 <2LENGTH: 6<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 237 Lys Trp Glu Glu Leu Ile ;2SEQ ID NO 238<2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 238 Ile Lys Lys Glu Trp Leu ;2SEQ ID NO 239 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 239 IleLys Asn Glu Trp Leu ;2SEQ ID NO 24LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 24ys Lys Glu Leu ;2SEQ ID NO 24LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 24ys Glu Lys Leu ;2SEQ ID NO 242 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 242 Ile Lys Asp Glu Trp Leu ;2SEQ ID NO 243 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 243 Ile Lys Gly Glu Trp Leu ;2SEQ ID NO 244 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 244 Ile Leu Glu Glu Trp Lys ;2SEQ ID NO 245 <2LENGTH: 32TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide Lys Gly Val Tyr Val Asp Glu Asp Asp Ala Gly Ile Tyr Ile Val Lys 2Ile Asp Asp Pro Arg Thr Leu Asn Lys Thr Val Tyr Ile Arg Pro 222et Asn Ile Leu Ser Gln Lys Glu Val Val Glu Ile Trp Glu Arg 225 234er GlyLeu Ser Leu Glu Lys Ile Tyr Val Ser Glu Asp Gln Leu 245 25eu Asn Met Lys Asp Lys Ser Tyr Val Glu Lys Met Ala Arg Cys His 267yr His Phe Phe Ile Lys Gly Asp Leu Tyr Asn Phe Glu Ile Gly 275 28ro Asn Ala Thr Glu Gly Thr Lys LeuTyr Pro Glu Val Lys Tyr Thr 29Met Asp Ser Tyr Met Glu Arg Tyr Leu 3<2SEQ ID NO 246 <2LENGTH: 32TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 246 Met Gly Glu Ser Lys Arg Thr Glu Lys Thr Arg Val Leu Val Val Gly Thr Gly Tyr Ile Gly Lys Arg Ile Val Arg Ala Cys Leu Ala Glu 2 Gly His Glu Thr Tyr ValLeu Gln Arg Pro Glu Ile Gly Leu Glu Ile 35 4u Lys Val Gln Leu Phe Leu Ser Phe Lys Lys Leu Gly Ala Arg Ile 5 Val Glu Gly Ser Phe Ser Asp His Gln Ser Leu Val Ser Ala Val Lys 65 7 Leu Val Asp Val Val Val Ser Ala Met Ser Gly Val His PheArg Ser 85 9s Asn Ile Leu Val Gln Leu Lys Leu Val Glu Ala Ile Lys Glu Ala Asn Val Lys Arg Phe Leu Pro Ser Glu Phe Gly Met Asp Pro Pro Met Gly His Ala Leu Pro Pro Gly Arg Glu Thr Phe Asp Gln Lys GluArg Gln Ala Ile Glu Ala Ala Gly Ile Pro Tyr Thr Tyr Val Val Gly Ala Cys Phe Ala Ala Tyr Phe Ala Gly Asn Leu Ser Gln Met Thr Leu Leu Pro Pro Lys Glu Lys Val Asn Ile Tyr Gly Asp Gly Val Lys Val Val Phe AlaAsp Glu Asp Asp Ile Ala Lys Tyr Thr 2Lys Thr Leu Asn Asp Pro Arg Thr Leu Asn Lys Thr Val Asn Ile 222ro Pro Asp Asn Val Leu Thr Gln Leu Glu Leu Val Gln Ile Trp 225 234ys Leu Thr Gly Lys Glu Leu Glu Lys Thr AsnIle Ala Ala Gln 245 25sp Phe Leu Ala Asn Ile Glu Gln Met Glu Ile Pro His Gln Ala Gly 267ly His Phe Tyr His Ile Phe Tyr Glu Gly Cys Leu Thr Asp His 275 28lu Val Gly Glu Asp Glu Glu Ala Ser Ser Leu Tyr Pro Asp Val Lys 29Lys Arg Met Asp Asp Tyr Leu Arg Met Phe Leu 332SEQ ID NO 247 <2LENGTH: 32TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 247 Met Ala Thr Glu Lys Ser Lys Ile Leu Val Ile Gly Gly Thr Gly Tyr Gly Lys Phe Leu Val Glu Ala Ser Ala Lys Ala Gly His Ser Thr 2 Phe Ala Leu Val Arg Glu Ala Thr LeuSer Asp Pro Val Lys Gly Lys 35 4r Val Gln Ser Phe Lys Asp Leu Gly Val Thr Ile Leu His Gly Asp 5 Leu Asn Asp His Glu Ser Leu Val Lys Ala Ile Lys Gln Val Asp Val 65 7 Val Ile Ser Thr Val Gly Ser Met Gln Ile Leu Asp Gln Thr Lys Ile 859e Ser Ala Ile Lys Glu Ala Gly Asn Val Lys Arg Phe Leu Pro Ser Phe Gly Val Asp Val Asp Arg Thr Ser Ala Val Glu Pro Ala Lys Ala Phe Ala Gly Lys Ile Gln Ile Arg Arg Thr Ile Glu Ala Glu Ile Pro Tyr ThrTyr Ala Val Thr Gly Cys Phe Gly Gly Tyr Tyr Leu Pro Thr Leu Val Gln Phe Glu Pro Gly Leu Thr Ser Pro Pro Arg Lys Val Thr Ile Leu Gly Asp Gly Asn Ala Lys Ala Val Ile Asn Glu Glu Asp Ile Ala Ala Tyr Thr IleLys Ala Val Asp Asp Pro 2Thr Leu Asn Lys Ile Leu Tyr Ile Lys Pro Ser Asn Asn Thr Leu 222et Asn Glu Ile Val Thr Leu Trp Glu Lys Lys Ile Gly Lys Ser 225 234lu Lys Thr His Leu Pro Glu Glu Gln Leu Leu Lys Ser IleGln 245 25lu Ser Pro Ile Pro Ile Asn Val Val Leu Ser Ile Asn His Ala Val 267al Asn Gly Asp Thr Asn Ile Ser Ile Glu Pro Ser Phe Gly Val 275 28lu Ala Ser Glu Leu Tyr Pro Asp Val Lys Tyr Thr Ser Val Asp Glu 29LeuSer Tyr Phe Ala 3<2SEQ ID NO 248 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 248 Tyr Gly Gly Phe Leu Arg Arg Gln Phe Lys Val Val Thr <2SEQ ID NO 249 <2LENGTH: 74 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 249 Lys Tyr Pro Lys Arg Ser Ser Glu Val Ala Gly Glu Gly Asp Gly Asp Met Gly His Glu Asp Leu Tyr Lys Arg Tyr Gly Gly Phe Leu Arg 2 Arg Ile Arg Pro Lys LeuLys Trp Asp Asn Gln Lys Arg Tyr Gly Gly 35 4e Leu Arg Arg Gln Phe Lys Val Val Thr Arg Ser Gln Glu Asp Pro 5 Asn Ala Tyr Ser Gly Glu Leu Phe Asp Ala 65 7SEQ ID NO 25LENGTH: 253 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 25la Trp Gln Gly Leu Val Leu Ala Ala Cys Leu Leu Met Phe Pro Thr ThrAla Asp Cys Leu Ser Arg Cys Ser Leu Cys Ala Val Lys 2 Thr Gln Asp Gly Pro Lys Pro Ile Asn Pro Leu Ile Cys Ser Leu Gln 35 4s Gln Ala Ala Leu Leu Pro Ser Glu Glu Trp Glu Arg Cys Gln Ser 5 Phe Ser Phe Phe Thr Pro Ser Thr Leu Gly Leu AsnAsp Lys Glu Asp 65 7 Leu Gly Ser Lys Ser Val Gly Glu Gly Pro Tyr Ser Glu Leu Ala Lys 85 9u Ser Gly Ser Phe Leu Lys Glu Leu Glu Lys Ser Lys Phe Leu Pro Ile Ser Thr Lys Glu Asn Thr Leu Ser Lys Ser Leu Glu Glu Lys Arg Gly Leu Ser Asp Gly Phe Arg Glu Gly Ala Glu Ser Glu Leu Arg Asp Ala Gln Leu Asn Asp Gly Ala Met Glu Thr Gly Thr Leu Tyr Leu Ala Glu Glu Asp Pro Lys Glu Gln Val Lys Arg Tyr Gly Gly Leu Arg Lys Tyr Pro Lys Arg Ser Ser Glu Val Ala Gly Glu Gly Gly Asp Ser Met Gly His Glu Asp Leu Tyr Lys Arg Tyr Gly Gly 2Leu Arg ArgIle Arg Pro Lys Leu Lys Trp Asp Asn Gln Lys Arg 222ly Gly Phe Leu Arg Arg Gln Phe Lys Val Val Thr Arg Ser Gln 225 234sp Pro Asn Ala Tyr Ser Gly Glu Leu Phe Asp Ala 245 25SEQ ID NO 25LENGTH: 2TYPE: DNA <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic oligonucleotide <4SEQUENCE: 25gccct ca 2SEQ ID NO 252<2LENGTH: 36 <2TYPE: DNA <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic oligonucleotide <4SEQUENCE: 252 tttctgccct cagaatttggagtagacgta gacaga 36 <2SEQ ID NO 253 <2LENGTH: 2;2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 253 Met Val Lys Lys Ile Ala Asn Asp Val Ser Asn Lys Leu Phe Pro Leu Lys Gly Phe Gly Asp Phe Val Gly Ile Glu Asp His Ile Lys Ala 2 Ile Lys Ser Ile Leu Cys Leu Glu Ser Lys Glu Ala Arg Ile Met Val 35 4y IleTrp Gly Gln Ser Gly Ile Gly Lys Ser Thr Ile Gly Arg Ala 5 Leu Phe Ser Gln Leu Ser Ser Gln Phe His His Arg Ala Phe Ile Thr 65 7 Tyr Lys Ser Thr Ser Gly Ser Asp Val Ser Gly Met Lys Leu Ser Trp 85 9u Lys Glu Leu Leu Ser Glu Ile Leu GlyGln Lys Asp Ile Lys Ile His Phe Gly Val Val Glu Gln Arg Leu Lys His Lys Lys Val Leu Leu Leu Asp Asp Val Asp Asn Leu Glu Phe Leu Lys Thr Leu Val Lys Ala Glu Trp Phe Gly Ser Gly Ser Arg Ile Ile Val Ile Thr Gln Asp Lys Gln Leu Leu Lys Ala His Glu Ile Asp Leu Val Tyr Glu Glu Leu Pro Ser Gln Gly Leu Ala Leu Lys Met Ile Ser Gln Tyr Phe Gly Lys Asp Ser Pro Pro Asp Asp Phe Lys Glu Leu Ala Phe 2ValAla Glu Leu Val Gly Ser Leu Pro Leu Gly Leu Ser Val Leu 222er Ser Leu Lys Gly Arg Asp Lys Asp Glu Trp Val Lys Met Met 225 234rg Leu Arg Asn Asp Ser Asp Asp Lys Ile Glu Glu Thr Leu Arg 245 25al Gly Tyr Asp Arg Leu AsnLys Lys Asn Arg Asp Asn Val Lys Glu 267eu Glu Asp Asp Val Gly Leu Thr Met Leu Ala Asp Lys Ser Leu 275 28le Arg Ile Thr Pro Asp Gly Asp Ile Glu Met His Asn Leu Leu Glu 29Leu Gly Arg Glu Ile Asp Arg Ala Lys Ser Lys GlyAsn Pro Ala 33Lys Arg Gln Phe Leu Thr Asn Phe Glu Asp Ile Gln Glu Val Val Thr 325 33lu Lys Thr Gly Thr Glu Thr Val Leu Gly Ile Arg Val Pro Pro Thr 345eu Phe Ser Thr Arg Pro Leu Leu Val Ile Asn Glu Glu Ser Phe 355 36ys Gly Met Gln Ile Gly Leu Trp Ser Lys Ile Asp Leu Pro Gln Gly 378al Tyr Leu Pro Leu Lys Leu Lys Leu Leu Lys Trp Asn Tyr Cys 385 39Leu Lys Ser Leu Pro Ser Thr Phe Lys Ala Glu Tyr Leu Val Asn 44Ile Met LysTyr Ser Lys Leu Glu Lys Leu Trp Glu Gly Thr Leu 423eu Gly Ser Leu Lys Lys Met Asp Leu Gly Cys Ser Asn Asn Leu 435 44ys Glu Ile Pro Asp Leu Ser Leu Ala Ile Asn Leu Glu Glu Leu Asn 456er Lys Cys Glu Ser Leu Val Thr LeuPro Ser Ser Ile Gln Asn 465 478le Lys Leu Arg Thr Leu Tyr Cys Ser Gly Val Leu Leu Ile Asp 485 49eu Lys Ser Leu Glu Gly Met Cys Asn Leu Glu Tyr Leu Ser Val Asp 55Ser Ser Met Glu Gly Thr Gln Gly Leu Ile Tyr Leu Pro ArgLys 5525 Leu Lys Arg Leu Trp Trp Asp Tyr Cys Pro Val Lys Arg Leu Pro Ser 534he Lys Ala Glu Tyr Leu Val Glu Leu Arg Met Glu Asn Ser Asp 545 556lu Lys Leu Trp Asp Gly Thr Gln Pro Leu Gly Ser Leu Lys Glu 565 57etTyr Leu His Gly Ser Lys Tyr Leu Lys Glu Ile Pro Asp Leu Ser 589la Ile Asn Leu Glu Arg Leu Tyr Leu Phe Gly Cys Glu Ser Leu 595 6Val Thr Leu Pro Ser Ser Ile Gln Asn Ala Thr Lys Leu Ile Asn Leu 662et Arg Asp Cys Lys LysLeu Glu Ser Phe Pro Thr Asp Leu Asn 625 634lu Ser Leu Glu Tyr Leu Asn Leu Thr Gly Cys Pro Asn Leu Arg 645 65sn Phe Pro Ala Ile Lys Met Gly Cys Ser Tyr Phe Glu Ile Leu Gln 667rg Asn Glu Ile Glu Val Glu Asp Cys Phe TrpAsn Lys Asn Leu 675 68ro Ala Gly Leu Asp Tyr Leu Asp Cys Leu Met Arg Cys Met Pro Cys 69Phe Arg Pro Glu Tyr Leu Thr Phe Leu Asp Val Ser Gly Cys Lys 77His Glu Lys Leu Trp Glu Gly Ile Gln Ile His Ala Leu Leu Asp Gly 72573yr Glu Leu Ala Gly His Leu Asp Gly Ser Ile Glu Thr Pro Ala Pro 745eu Thr Thr Asn Asn Val Val Ser Ala Asn Pro Gln Tyr Thr Leu 755 76rp Lys Arg Gln Asp Arg Leu Ile Phe Ser Ala Leu Ile Gly Ala Ile 778ro Pro ValGln Pro Leu Val Ser Arg Ala Thr Lys Ala Ser Gln 785 79Trp Lys Thr Leu Thr Asn Thr Tyr Ala Lys Ser Ser Tyr Asp His 88Lys Gln Leu Arg Thr Gln Ile Lys Gln Leu Lys Lys Gly Thr Lys 823le Asp Glu Tyr Val Leu Ser HisThr Thr Leu Leu Asp Gln Leu 835 84la Ile Leu Gly Lys Pro Met Glu His Glu Glu Gln Val Glu Arg Ile 856lu Gly Leu Pro Glu Asp Tyr Lys Thr Val Val Asp Gln Ile Glu 865 878ys Asp Asn Thr Pro Ser Ile Thr Glu Ile His Glu ArgLeu Ile 885 89sn His Glu Ala Lys Leu Leu Ser Thr Ala Ala Leu Ser Ser Ser Ser 99Pro Met Ser Ala Asn Val Ala Gln Gln Arg His His Asn Asn Asn 9925 Arg Asn Asn Asn Gln Asn Lys Asn Arg Thr Gln Gly Asn Thr Tyr Thr 934sn Trp Gln Pro Ser Ala Asn Asn Lys Ser Gly Gln Arg Pro Phe 945 956ro Tyr Leu Gly Lys Cys Gln Ile Cys Asn Val Gln Gly His Ser 965 97la Arg Arg Cys Pro Gln Leu Gln Ala Met Gln Pro Ser Ser Ser Ser 989la Ser Thr Phe ThrPro Trp Gln Pro Arg Ala Asn Leu Ala Met 995 Ala Pro Tyr Thr Ala Asn Asn Trp Leu Leu Asp Ser Gly Ala Thr His His Ile Thr Ser Asp Leu Asn Ala Leu Ala Leu His Gln 3Pro Tyr Asn Gly Asp Asp Val Met Ile Ala Asp Gly Thr Ser Leu 45 s Ile Thr Lys Thr Gly Ser Thr Phe Leu Pro Ser Asn Ala Arg 6Asp Leu Thr Leu AsnLys Val Leu Tyr Val Pro Asp Ile Gln Lys 75 n Leu Val Ser Val Tyr Arg Leu Cys Asn Thr Asn Gln Val Ser 9Val Glu Phe Phe Pro Ala Ser Phe Gln Val Lys Asp Leu Asn Thr Gly Thr Leu Leu Leu Gln Gly Arg Thr Lys Asp GluLeu Tyr Glu 2Trp Pro Val Thr Asn Pro Lys Ala Thr Ala Leu Phe Thr Thr Pro 35 r Pro Lys Thr Thr Leu Ser Ser Trp His Ser Arg Leu Gly His 5Pro Ser Ser Ser Ile Leu Asn Thr Leu Ile Ser Lys Phe Ser Leu 65 o Val Ser Val Ser Ala Ser Asn Lys Leu Ala Cys Ser Asp Cys 8Phe Ile Asn Lys Ser His Lys Leu Pro Phe Ser Ile Ser Ser Ile 95 s Ser Thr Ser Pro Leu Glu Tyr Ile Phe Ser Asp Val Trp Met Ser Pro Ile Leu Ser Pro AspAsn Tyr Lys Tyr Tyr Leu Gln Lys 25 r Gln Val Lys Ser Thr Phe Ile Ala Phe Lys Ala Leu Val Glu 4Asn Arg Phe Gln Ala Lys Ile Arg Thr Leu Tyr Ser Asp Asn Gly 55 y Glu Phe Ile Ala Leu Arg Glu Phe Leu Val Ser Asn GlyIle 7Ser His Leu Thr Ser Pro Pro His Thr Pro Glu His Asn Gly Leu 85 r Glu Arg Lys His Arg His Ile Val Glu Thr Gly Leu Thr Leu Leu Thr Gln Ala Ser Val Pro Arg Glu Tyr Trp Pro Tyr Ala Phe Ala AlaAla Val Tyr Leu Ile Asn Arg Met Pro Thr Pro Val Leu 3Ser Met Glu Ser Pro Phe Gln Lys Leu Phe Gly Ser Lys Pro Asn 45 r Glu Arg Leu Arg Val Phe Gly Cys Leu Cys Phe Pro Trp Leu 6Arg Pro Tyr Thr His Asn Lys Leu GluGlu Arg Ser Arg Arg Cys 75 l Phe Leu Gly Tyr Ser Thr Gln Thr Ala Tyr Leu Cys Phe Asp 9Val Glu His Lys Arg Leu Tyr Thr Ser Arg His Val Val Phe Asp Glu Ala Ser Phe Pro Phe Ser Asn Leu Thr Ser Gln Asn Ser Leu 2Pro Thr Val Thr Phe Glu Gln Ser Ser Ser Pro Leu Val Thr Pro 35 e Leu Ser Ser Ser Ser Val Leu Pro Ser Cys Leu Ser Ser Pro 5Cys Thr Val Leu His Gln Gln Gln Pro Pro Val Thr Thr Pro Asn 65 r Pro His Ser SerGln Pro Thr Thr Ser Pro Ala Pro Leu Ser 8Pro His Arg Ser Thr Thr Met Asp Phe Gln Val Pro Gln Pro Thr 95 a Pro Asn Glu Asn Gly Pro Glu Pro Glu Ala Gln Ser Pro Pro Ile Gly Pro Leu Ser Asn Pro Thr His Glu Ala PheIle Gly Pro 25 u Pro Asn Pro Asn Arg Asn Pro Thr Asn Glu Ile Glu Pro Thr 4Pro Ala Pro His Pro Lys Pro Val Lys Pro Thr Thr Thr Thr Thr 55 r Pro Asn Arg Thr Thr Val Ser Asp Ala Ser His Gln Pro Thr 7Ala Pro Gln Gln Asn Gln His Asn Met Lys Thr Arg Ala Lys Asn 85 n Ile Lys Lys Pro Asn Thr Lys Phe Ser Leu Thr Ala Thr Leu Pro Asn Arg Ser Pro Ser Glu Pro Thr Asn Val Thr Gln Ala Leu Lys Asp Lys Lys Trp Arg PheAla Met Ser Asp Glu Phe Asp Ala 3Gln Gln Arg Asn His Thr Trp Asp Leu Val Pro His Glu Ser Gln 45 u Leu Val Gly Cys Lys Trp Val Phe Lys Leu Lys Tyr Leu Pro 6Asn Gly Ala Ile Asp Lys Tyr Lys Ala Arg Leu Val Ala LysGly 75 e Asn Gln Gln Tyr Gly Val Asp Tyr Ala Glu Thr Phe Ser Pro 9Val Ile Lys Ser Thr Thr Ile Arg Leu Val Leu Asp Val Ala Val Lys Lys Asp Trp Glu Ile Lys Gln Leu Asp Val Asn Asn Ala Phe 2Leu GlnGly Thr Leu Thr Glu Glu Val Tyr Met Ala Gln Pro Pro 35 y Phe Ile Asp Lys Asp Arg Pro Thr His Val Cys Arg Leu Arg 5Lys Ala Ile Tyr Gly Leu Lys Gln Ala Pro Arg Ala Trp Tyr Met 65 u Leu Lys Gln His Leu Phe Asn IleGly Phe Val Asn Ser Leu 8Ser Asp Ala Ser Leu Phe Ile Tyr Trp Ser Asp Lys Ser Ser Ile 95 p Ala Val Leu Thr Ser Leu Ala Glu Arg Phe Ser Ile Lys Asp Pro Thr Asp Leu His Tyr Phe Leu Gly Ile Glu Ala Thr Arg Thr 25 s Gln Gly Leu His Leu Met Gln Arg Lys Tyr Ile Lys Asp Leu 4Leu Ala Lys His Asn Met Ala Asp Ala Lys Pro Val Leu Thr Pro 55 u Pro Thr Ser Pro Lys Leu Thr Leu His Gly Gly Thr Lys Leu 7Asn Asp Ala Ser GluTyr Arg Ser Val Val Gly Ser Leu Gln Tyr 85 u Ala Phe Thr Arg Pro Asp Ile Ala Tyr Ala Val Asn Arg Leu Ser Gln Leu Met Pro Gln Pro Thr Glu Asp His Trp Gln Ala Ala Lys Arg Val Leu Arg Tyr Leu Ala Gly Thr Ser ThrHis Asp Trp 3Ala Gly Asp Ser Asp Asp Tyr Val Ser Thr Asn Ala Tyr Val Ile 45 r Leu Gly Lys Asn Pro Ile Ser Trp Ser Ser Lys Lys Gln Arg 6Gly Val Ala Arg Ser Ser Thr Glu Ser Glu Tyr Arg Ala Val Ala 75 n Ala Ala Ser Glu Val Lys Trp Leu Cys Ser Leu Leu Ser Lys 9Leu His Ile Arg Leu Pro Ile Arg Pro Ser Ile Phe Cys Asp Asn 25 2 Gly Ala Thr Tyr Leu Cys Ala Asn Pro Val Phe His Ser Arg 2Met Lys His Ile Ala Ile AspTyr His Phe Val Arg Asn Met Ile 25 2 Ser Gly Ala Leu Arg Val Ser His Val Ser Thr Arg Asp Gln 2Leu Ala Asp Ala Leu Thr Lys Pro Leu Ser Arg Ala His Phe Gln 25 2 Ala Arg Phe Lys Ile Gly Val Arg Gln Leu Pro Pro Ser2<2SEQ ID NO 254 <2LENGTH: 575 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide Ala His Ala Leu Lys Thr Lys Glu Lys Leu Ala Gln Thr Ala Thr Ala Ser Ser Ala Ala Val Gly Ser Gly Pro Pro Pro Glu Ala Glu Gln Ala Pro Gln Ser Ser Gly Glu Glu Glu Leu Gln Leu Gln Leu Ala Leu Met SerLys Glu Glu Ala Asp Gln Pro Pro Ser Cys Gly Pro Glu 2Asp Val Gln Leu Gln Leu Ala Leu Ser Leu Ser Arg Glu Glu His 222ys Glu Glu Arg Ile Arg Arg Gly Asp Asp Leu Arg Leu Gln Met 225 234le Glu Glu Ser Lys Arg GluThr Gly Gly Lys Glu Glu Ser Ser 245 25eu Met Asp Leu Ala Asp Val Phe Thr Thr Pro Ala Pro Pro Gln Ala 267sp Pro Trp Gly Gly Pro Ala Ser Val Pro Thr Ala Val Pro Val 275 28la Ala Ala Ala Ser Asp Pro Trp Gly Ala Pro Ala Val ProPro Ala 29Asp Pro Trp Gly Gly Ala Ala Pro Thr Pro Ala Ser Gly Asp Pro 33Trp Arg Pro Ala Ala Pro Thr Gly Pro Ser Val Asp Pro Trp Gly Gly 325 33hr Pro Ala Pro Ala Ala Gly Glu Gly Pro Thr Ser Asp Pro Trp Gly 345la Asp Gly Gly Ala Pro Val Ser Gly Pro Pro Ser Ser Asp Pro 355 36rp Ala Pro Ala Pro Ala Phe Ser Asp Pro Trp Gly Gly Ser Pro Ala 378ro Ser Ser Asn Gly Thr Ala Val Gly Gly Phe Asp Thr Glu Pro 385 39Glu Phe Ser AspPhe Asp Arg Leu Arg Thr Ala Leu Pro Thr Ser 44Ser Ser Thr Gly Glu Leu Glu Leu Leu Ala Gly Glu Val Pro Ala 423er Pro Gly Ala Phe Asp Met Ser Gly Val Gly Gly Ser Leu Ala 435 44lu Ser Val Gly Ser Pro Pro Pro Ala Ala ThrPro Thr Pro Thr Pro 456hr Arg Lys Thr Pro Glu Ser Phe Leu Gly Pro Asn Ala Ala Leu 465 478sp Leu Asp Ser Leu Val Ser Arg Pro Gly Pro Thr Pro Pro Gly 485 49la Lys Ala Ser Asn Pro Phe Leu Pro Ser Gly Ala Pro Ala Thr Gly55Ser Val Thr Asn Pro Phe Gln Pro Ala Pro Pro Ala Thr Leu Thr 5525 Leu Asn Gln Leu Arg Leu Ser Pro Val Pro Pro Val Pro Gly Ala Pro 534hr Tyr Ile Ser Pro Leu Gly Gly Gly Pro Gly Leu Pro Pro Met 545 556roPro Gly Pro Pro Ala Pro Asn Thr Asn Pro Phe Leu Leu 565 57lt;2SEQ ID NO 255 <2LENGTH: 92TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 255 Met Glu Pro Pro Leu Pro Val Gly Ala Gln Pro Leu Ala Thr Val Glu Met Glu Met Lys Gly Pro Leu Arg Glu Pro Cys Ala Leu Thr Leu 2 Ala Gln Arg Asn Gly Gln Tyr Glu LeuIle Ile Gln Leu His Glu Lys 35 4u Gln His Val Gln Asp Ile Ile Pro Ile Asn Ser His Phe Arg Cys 5 Val Gln Glu Ala Glu Glu Thr Leu Leu Ile Asp Ile Ala Ser Asn Ser 65 7 Gly Cys Lys Ile Arg Val Gln Gly Asp Trp Ile Arg Glu Arg Arg Phe 859u Ile Pro Asp Glu Glu His Cys Leu Lys Phe Leu Ser Ala Val Leu Ala Gln Lys Ala Gln Ser Gln Leu Leu Val Pro Glu Gln Lys Asp Ser Ser Trp Tyr Gln Lys Leu Asp Thr Lys Asp Lys Pro Ser Val Ser Gly Leu LeuGly Phe Glu Asp Asn Phe Ser Ser Met Asn Leu Asp Lys Lys Ile Asn Ser Gln Asn Gln Pro Thr Gly Ile His Arg Glu Pro Pro Pro Pro Phe Ser Val Asn Lys Met Leu Pro Arg Glu Lys Ala Ser Asn Lys Glu Gln Pro Lys ValThr Asn Thr Met Arg Lys 2Phe Val Pro Asn Thr Gln Ser Gly Gln Arg Glu Gly Leu Ile Lys 222le Leu Ala Lys Arg Glu Lys Glu Tyr Val Asn Ile Gln Thr Phe 225 234he Phe Val Gly Thr Trp Asn Val Asn Gly Gln Ser Pro AspSer 245 25ly Leu Glu Pro Trp Leu Asn Cys Asp Pro Asn Pro Pro Asp Ile Tyr 267le Gly Phe Gln Glu Leu Asp Leu Ser Thr Glu Ala Phe Phe Tyr 275 28he Glu Ser Val Lys Glu Gln Glu Trp Ser Met Ala Val Glu Arg Gly 29HisSer Lys Ala Lys Tyr Lys Lys Val Gln Leu Val Arg Leu Val 33Gly Met Met Leu Leu Ile Phe Ala Arg Lys Asp Gln Cys Arg Tyr Ile 325 33rg Asp Ile Ala Thr Glu Thr Val Gly Thr Gly Ile Met Gly Lys Met 345sn Lys Gly Gly Val AlaVal Arg Phe Val Phe His Asn Thr Thr 355 36he Cys Ile Val Asn Ser His Leu Ala Ala His Val Glu Asp Phe Glu 378rg Asn Gln Asp Tyr Lys Asp Ile Cys Ala Arg Met Ser Phe Val 385 39Pro Asn Gln Thr Leu Pro Gln Leu Asn Ile MetLys His Glu Val 44Ile Trp Gly Asp Leu Asn Tyr Arg Leu Cys Met Pro Asp Ala Asn 423al Lys Ser Leu Ile Asn Lys Lys Asp Leu Gln Arg Leu Leu Lys 435 44he Asp Gln Leu Asn Ile Gln Arg Thr Gln Lys Lys Ala Phe Val Asp 456sn Glu Gly Glu Ile Lys Phe Ile Pro Thr Tyr Lys Tyr Asp Ser 465 478hr Asp Arg Trp Asp Ser Ser Gly Lys Cys Arg Val Pro Ala Trp 485 49ys Asp Arg Ile Leu Trp Arg Gly Thr Asn Val Asn Gln Leu Asn Tyr 55Ser His MetGlu Leu Lys Thr Ser Asp His Lys Pro Val Ser Ala 5525 Leu Phe His Ile Gly Val Lys Val Val Asp Glu Arg Arg Tyr Arg Lys 534he Glu Asp Ser Val Arg Ile Met Asp Arg Met Glu Asn Asp Phe 545 556ro Ser Leu Glu Leu Ser Arg ArgGlu Phe Val Phe Glu Asn Val 565 57ys Phe Arg Gln Leu Gln Lys Glu Lys Phe Gln Ile Ser Asn Asn Gly 589al Pro Cys His Phe Ser Phe Ile Pro Lys Leu Asn Asp Ser Gln 595 6Tyr Cys Lys Pro Trp Leu Arg Ala Glu Pro Phe Glu Gly Tyr LeuGlu 662sn Glu Thr Val Asp Ile Ser Leu Asp Val Tyr Val Ser Lys Asp 625 634al Thr Ile Leu Asn Ser Gly Glu Asp Lys Ile Glu Asp Ile Leu 645 65al Leu His Leu Asp Arg Gly Lys Asp Tyr Phe Leu Thr Ile Ser Gly 667yr Leu Pro Ser Cys Phe Gly Thr Ser Leu Glu Ala Leu Cys Arg 675 68et Lys Arg Pro Ile Arg Glu Val Pro Val Thr Lys Leu Ile Asp Leu 69Glu Asp Ser Phe Leu Glu Lys Glu Lys Ser Leu Leu Gln Met Val 77Pro Leu Asp Glu Gly AlaSer Glu Arg Pro Leu Gln Val Pro Lys Glu 725 73le Trp Leu Leu Val Asp His Leu Phe Lys Tyr Ala Cys His Gln Glu 745eu Phe Gln Thr Pro Gly Met Gln Glu Glu Leu Gln Gln Ile Ile 755 76sp Cys Leu Asp Thr Ser Ile Pro Glu Thr Ile ProGly Ser Asn His 778al Ala Glu Ala Leu Leu Ile Phe Leu Glu Ala Leu Pro Glu Pro 785 79Ile Cys Tyr Glu Leu Tyr Gln Arg Cys Leu Asp Ser Ala Tyr Asp 88Arg Ile Cys Arg Gln Val Ile Ser Gln Leu Pro Arg Cys His Arg 823al Phe Arg Tyr Leu Met Ala Phe Leu Arg Glu Leu Leu Lys Phe 835 84er Glu Tyr Asn Ser Val Asn Ala Asn Met Ile Ala Thr Leu Phe Thr 856eu Leu Leu Arg Pro Pro Pro Asn Leu Met Ala Arg Gln Thr Pro 865 878sp Arg Gln Arg Ala Ile Gln Phe Leu Leu Gly Phe Leu Leu Gly 885 89er Glu Glu Asp 92SEQ ID NO 256 <2LENGTH: t;2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 256 Met Ser Glu Ser Gly Asn Thr Thr Ser Met Pro Gly Cys Gly Arg Met Ala Leu Arg Ser Thr Trp Ser Lys Arg Ala Phe Leu Val Ala Cys 2 Lys Asp Gly Ala Leu Thr Ser Asp Gly Arg Cys Pro Gln Tyr Gly Cys 35 4y AlaLeu Val Ser Ile Thr Lys Gly Val Gln Gln Pro Lys Lys Thr 5 Ala Ser Ala Lys Val Val Lys Cys Leu Cys Trp Val Gln Pro Ala Arg 65 7 Trp Cys Glu Lys His Ser Lys Gly Pro Ala Ser Pro Asn Gly Ser Val 85 9r Thr Lys Arg Ser Asn Ser Ala Arg AlaAla Pro Ala Pro Leu Pro Lys Lys Gln Thr Cys Asp Val Val Val Thr Val Gly Pro Leu Glu Val Tyr Pro Ala Leu Val Ser Glu Glu Leu Pro Thr Pro Val Ala Thr Pro Thr Lys Val Glu Glu Val Pro Ile Pro Glu Leu Pro Leu Trp Leu Ala Pro Ala Trp Met Val Glu Gln Pro Tyr Ala Ala Thr Pro Val Leu Cys Leu Thr Gln Arg Glu Glu Phe Ala Leu Leu Lys Lys Leu Thr Arg Lys Gly Lys Leu Leu Gln Arg Arg Ala Thr His Ala 2PheGlu Ala Arg Ala Ala Leu Ala Arg Val Arg Ala Ala Thr Gln 222ys Val Glu Glu Val Thr Ala Leu Val Ile Lys Gly Arg Arg Ile 225 234la Ala His Gln Leu Leu Arg Glu Leu Glu Glu Val Ala Pro Leu 245 25er Gln Ala Gln Glu Gln LeuVal Ala Ser Ser Cys Ala Ala Ala Ala 267rg Gln Glu Glu Cys Ala Ser Phe Leu Arg Arg Ala Lys Ala Trp 275 28rg Lys Ser Ile Ser Ala Thr Pro Pro Val Ala Ala Thr Ala Val Ala 29Lys Val Val Ser Ala Thr Met Pro Trp Ala His LeuGly Leu Ser 33Leu Gly Gly Leu Leu Ala Val Pro Thr Leu Asp Gly Thr Leu Gly Ala 325 33ys Gln Trp Asn Ala Lys Thr Ile Ala Thr Trp Val Leu Lys Pro Val 345er Cys Val Gln Ser Val His Ala Lys Val Arg Asp Trp Leu His 355 36er Gln Pro Glu Val Gly Val Thr Asn Thr Lys Val Pro Leu Val Leu 378lu Val Cys Leu Gly Val Leu Ser Pro Pro Ser Leu Ser Glu Glu 385 39Val Asp Asn Pro Gln Glu Thr Ser Gln Ser Gly Ile Trp His Pro 44Met Gly ValArg Asn Ile Tyr Val Phe His Asp Asp Ser Trp Glu 423er Pro Glu Glu Asp Glu Asn Tyr Thr Tyr Thr Phe Ser Arg Gln 435 44ys Gly Ile Pro Tyr Leu Leu Val Glu Gly Arg Gly Ala Glu Glu Arg 456sn Thr Ile Leu Gly Trp Asp Phe SerLeu His Asn Asp Gly Phe 465 478he Leu Pro Ser Pro Glu Glu Gly Tyr Thr Lys Glu Leu Val Thr 485 49ro Val Ala Leu Glu Glu Glu Asp Lys Tyr Ser Thr Ala Ser Ser Cys 55Phe Phe Ser Leu Asp Asp Val Ser Ser Ala Ile Thr Ile GlnCys 5525 Pro Gly Leu Leu Ser Ala Asp Ala Asp Val His Phe Phe Asp Gly Pro 534yr Arg Cys Ser Ser Arg Pro Arg Asp Phe Arg Pro Pro Val Val 545 556ly Cys Asp Tyr Glu Ser Arg Val Lys Ala Ser Ile Gln Arg Lys 565 57leGlu Asn Pro Leu Gln Glu Arg Phe Ile Thr Val Leu Arg Glu Lys 589ys Lys Asn Lys Lys Lys Glu Phe His Ser Phe Ser Ala Cys Phe 595 6Ala Phe Lys Arg Lys Gln Ile Gln Trp Pro Pro Thr Pro Asn Glu Met 662sn Glu Trp Glu Glu TyrCys Ile Ala Gln Ala Trp Leu Pro Phe 625 634al Val Val Thr Asp Glu Ile Glu Asp Val Thr Pro Leu Tyr Pro 645 65ly Gly Arg Asp Tyr Asn Cys Asn Ser Gln Leu Leu Phe Pro Leu Ala 667eu Ser Thr Val Tyr Cys Asp Asp Ser Cys PheHis Pro Asn Asp 675 68ly Trp Thr Thr Asp Gly Asn Gly Lys His Phe Arg Leu Ser Pro Gln 69Val Leu Pro Asp Val Pro Ile Pro Ile Val His Arg Val Thr Arg 77Gln Leu Pro Gln Phe Leu Tyr Asp Leu Gly Ile Gly Asp Leu Thr Cys 72573sn Ser Gly Tyr Gln Ala Glu Asn Leu Gln Glu Glu Ile Gln Glu Arg 745lu Asp Arg Ser Glu Glu Lys Pro Val Pro Ser Leu Asp Thr Leu 755 76le Ser Lys Leu Ser Lys Arg Ser Thr Lys Val Lys Gly Ala Gly Glu 778rg Tyr AlaAsp Arg His Ser Leu Thr Glu Lys Ala Ile Phe His 785 79Pro Gly Ala Leu Ser Arg Met Arg Ser Gly Lys Glu Lys Thr Ile 88Ala Ala Asn His Asn Ser Asp Gln Ile Ser Val Arg Met Ala Glu 823ly Lys Pro Val Phe Thr Pro LeuPro Arg Met Ser Asp Glu Met 835 84eu Arg Lys Phe Leu Glu Lys Gly Leu Gly Ser Thr Ser Thr Val Ala 856sp Ile Gly Ile Gln Ser His Ile Pro Gln Gly Met Pro Thr Val 865 878he Val Asn Val Met Asp Thr Arg Ile Glu Asp Pro LeuTyr Ser 885 89er Leu Cys Gly Ser Tyr Ile Asp Leu Gly Arg Asp Arg Ala Lys Thr 99Cys Leu Pro Leu Val Asn Phe Pro Met Ser Lys Leu Ala Glu Asp 9925 Val Asp Asp Val Leu Asn Gly Leu Met Leu Cys Thr His Phe Gln Asp 934hr Lys Phe Gly Val Gly Lys Pro Ala Phe Gln Tyr Gly Thr Leu 945 956he Gln Glu Phe Lys Pro Ser Ala Tyr Ser Asp Phe Ser Arg Val 965 97rg Asp Asn Trp Asp Ala Ile Ala Lys Gln Gln Asn Thr Pro Asn Asp 989le Leu Ala Gly PheSer Val Leu Gly Ala Val Ser Gln Ala Tyr 995 Gln Ala Leu Pro Val Phe Lys Ser Val Glu Leu Val Ala Pro Pro Lys Arg Lys Pro Val Val Ala Thr Phe Gln Asn Pro Thr Thr 3Leu Gly Arg Ser Asn Thr Thr Arg Ser Phe Arg MetPro Thr Met 45 p Leu Pro Arg Ser Thr Gly Arg Asp Ala Pro Ile Pro Ile Val 6His Arg Arg Asn Asn Asn Asp Val His Phe Asp Glu Ala Thr Pro 75 a Arg Phe Ser Thr Cys Asp Ser Gly Leu Val Ala Asp Thr Thr 9Leu Ala Phe Ala Lys Met Tyr Gln Cys Lys Lys Asp Ala Lys Ala Gly His Val Leu Ala Thr Ile Asp Ile Gln Glu Cys Val Phe Glu 2Asp Asn Arg Arg Val Ala Leu Asp Trp Leu Ala His Gly Leu Ala 35 r Phe Lys Tyr Asp Leu GlnLeu Thr Val Asp Ser Asn Pro Phe 5Val Gly Val Thr Leu Gly Ile Thr Val Asp Ala Phe Asp Arg Leu 65 u Pro Gln Ile Ser Asp Glu Val Ile Ala Val Pro Leu Ala Phe 8 Gln Leu Pro Thr Tyr Leu Phe Pro Ile Ser Lys Lys Gly Thr Phe 95 r Gln Thr Ile Asp Phe Ala Ala Ile Ala Gly Tyr Asn Phe Phe Pro His Val Ala Ala Phe Gly Arg Pro Lys Ile Ile Val Tyr Ile 25 l Ser Asp Asn AspLeu Pro Ala Ser Asp Thr Trp Met Cys Leu 4Val Glu Leu His Met Thr Arg Leu Glu Ser Ser Thr Leu Ala Cys 55 r Pro Thr Leu Val Leu Pro Gln Ala Phe Gly Gly Asp Leu Pro 7Leu Asp Leu Trp Arg Gly Pro Tyr Thr Phe Pro LeuGly Gly Gly 85 r Lys Arg Leu Ser Thr Ser Leu Asp Ile Gly Thr Ser Thr Thr Thr Val Ser Gly Trp Arg Thr Val Ser Pro Ala Ala Tyr Ala Leu Phe Leu Gln Gly His Gly Gly Ser Leu Val Gly Glu Val Val His 3Thr Gly Ser Ala Ala Val Ser Cys Ala Leu His Leu Cys Ile Ser 45 e Gly Gly Ala Pro Pro Thr Leu Glu Glu Ala Leu Val Phe Pro 6Gly Phe Arg Leu Pro Ser Gly Glu Gly Lys Phe His Ile Lys Val 75 n Thr Pro Tyr Gly Arg LeuSer Thr Leu Thr Pro Asp Cys Ala 9Leu Tyr Val Tyr Leu Ala Gly Gly Pro Ile Ala Val Ala Pro Met Ser Val Pro Tyr Gln Phe Cys Ile His Leu Glu Arg Leu Val Asp 2Asp Gly Ala Pro Pro Arg Thr Ile Gly Leu Ile Arg Glu PheAsn 35 p Ala Thr Ile Asn Asn Phe Lys Ser Asp Asp Ile Thr Phe Ala 5Ile Pro Ala Arg Leu Ser Asp Leu Val Leu Thr Cys Gly Asp Val 65 r Met Ser Thr Asn Pro Leu Ala Leu Leu Ile Gly Ser Cys Gly 8Phe PheArg Gly Asn Leu Thr Val Val Leu Glu Trp Ala Thr Phe 95 u Lys Ala Gly Asp Lys Glu Gly Thr Val Gln Leu Thr Thr Cys Arg Gly Met Ile Asn Asn Val Lys Gly Val Arg Asn Ala Ile Gln 25 s Lys Val Val Asn Leu Ser Leu ValGly Ser Val Ser Arg Tyr 4Leu Asn Val Gly Asp Phe Thr Gly Phe Ala Gln Ser Gly Gly Gln 55 l Gly Tyr Asp Glu Ile Phe Leu Glu Phe Ser Thr Asn Lys Ala 7Lys Gln Ile Arg Tyr Leu Asn Ile Asn Val Glu Leu Asp Glu Asn 85 e Glu Leu Tyr Gly Arg Thr Ile Ile Pro Leu Lys Asn Thr Ala Pro Ala Phe Ala Ser Thr Ser Ser Ala Pro Asn Glu Ser <2SEQ ID NO 257 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 257 Lys Phe Leu Pro Ser ;2SEQ ID NO 258 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 258 Phe Leu Pro Ser Ile ;2SEQ ID NO 259 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 259 Arg Phe Leu Pro Ser ;2SEQ ID NO 26LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 26eu Pro Ser Glu ;2SEQ IDNO 26LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 26he Leu Lys SEQ ID NO 262 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 262 TrpGlu Arg Cys SEQ ID NO 263 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 263 Phe Ser Phe Phe Thr Pro ;2SEQ ID NO 264 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 264 Phe Phe Asn Pro SEQ ID NO 265 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 265 Phe Pro Ser Thr SEQ ID NO 266 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 266 Ser Phe Leu Gly SEQ ID NO 267 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <2SEQ ID NO 268 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE:268 Ser Tyr Leu Gly SEQ ID NO 269 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 269 Ser Trp Leu Gly SEQ ID NO 27LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 27he Thr Pro Ser ;2SEQ ID NO 27LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 27he Leu Ser Phe Phe Thr Pro Ser ;2SEQ ID NO 272 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 272 Asn Pro Phe Gln Pro ;2SEQ ID NO 273 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 273 Met Ser Phe Leu Lys ;2SEQ ID NO 274 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 274 Phe Leu Pro Pro Pro Ser ;2SEQ ID NO 275 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 275 Phe Leu Pro Pro Ser ;2SEQ ID NO 276 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 276 Met Phe Pro Ser Thr ;2SEQ ID NO 277 <2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 277 Phe Leu Pro Pro Pro Pro Pro Pro Ser ;2SEQ ID NO 278 <2LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 278 PheLeu Pro Pro Pro Pro Pro Ser ;2SEQ ID NO 279 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 279 Phe Gly Gly Phe Ile Met ;2SEQ ID NO 28LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 28eu Phe Ser SEQ ID NO 28LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 28rg Glu Trp SEQ ID NO 282 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 282 Pro Thr Phe Phe Ser Phe ;2SEQ ID NO 283 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 283 Pro Asn Phe Phe SEQ ID NO 284 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 284 Thr Ser Pro Phe SEQ ID NO 285 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence:Synthetic polypeptide <4SEQUENCE: 285 Gly Leu Phe Ser SEQ ID NO 286 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 286 Leu Glu Ser Tyr SEQ ID NO 287 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 287 Gly Leu Tyr Ser SEQ ID NO 288 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 288 Gly Leu Trp Ser SEQ ID NO 289 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 289 Ser Pro Thr Phe Phe ;2SEQ ID NO 29LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 29ro Thr Phe Phe Ser Leu Phe Ser ;2SEQ ID NO 29LENGTH: 5 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 29ln Phe Pro Asn ;2SEQ ID NO 292 <2LENGTH: 5<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 292 Lys Leu Phe Ser Met ;2SEQ ID NO 293<2LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 293 Ser Pro Pro Pro Pro Leu Phe ;2SEQ ID NO 294 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 294 SerPro Pro Leu Phe ;2SEQ ID NO 295 <2LENGTH: 5 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 295 Thr Ser Pro Phe Met ;2SEQ ID NO 296 <2LENGTH: 2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 296 Ser Pro Pro Pro Pro Pro Pro Pro Leu Phe <2SEQ ID NO 297 <2LENGTH: 9 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 297 Ser Pro Pro Pro Pro Pro Pro Leu Phe ;2SEQ ID NO 298 <2LENGTH: 6 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 298 Met Ile Phe Gly Gly Phe ;2SEQ ID NO 299 <2LENGTH: ;2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide Lys Leu Arg Gly Leu Ser Asp Gly Phe Arg Glu Gly Ala Glu Ser Glu Met Arg Asp Ala Gln Leu Asn Asp Gly Ala Met Glu Thr Gly Thr Leu Tyr Leu Ala Glu Glu Asp Pro Lys Glu Gln Val Lys Arg <2SEQ ID NO 32LENGTH: ;2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Ala Arg Phe Leu Thr LeuCys Thr Trp Leu Leu Leu Leu Gly Pro Leu Leu Ala Thr Val Arg Ala Glu Cys Ser Gln Asp Cys Ala Thr 2 Cys Ser Tyr Arg Leu Val Arg Pro Ala Asp Ile Asn Phe Leu Ala Cys 35 4l Met Glu Cys Glu Gly Lys Leu Pro Ser Leu Lys Ile Trp GluThr 5 Cys Lys Glu Leu Leu Gln Leu Ser Lys Pro Glu Leu Pro Gln Asp Gly 65 7 Thr Ser Thr Leu Arg Glu Asn Ser Lys Pro Glu Glu Ser His Leu Leu 85 9a Lys Arg Tyr ;2SEQ ID NO 32LENGTH: 267 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Ala Arg Phe Leu Thr Leu Cys Thr Trp Leu Leu Leu Leu Gly Pro Leu Leu Ala Thr Val Arg Ala Glu Cys Ser Gln Asp Cys Ala Thr 2 Cys Ser Tyr Arg Leu Val Arg Pro Ala Asp Ile Asn Phe Leu Ala Cys 35 4l Met Glu Cys Glu Gly Lys Leu Pro Ser Leu Lys Ile Trp Glu Thr 5 Cys Lys Glu Leu Leu Gln Leu Ser LysPro Glu Leu Pro Gln Asp Gly 65 7 Thr Ser Thr Leu Arg Glu Asn Ser Lys Pro Glu Glu Ser His Leu Leu 85 9a Lys Arg Tyr Gly Gly Phe Met Lys Arg Tyr Gly Gly Phe Met Lys Met Asp Glu Leu Tyr Pro Met Glu Pro Glu Glu Glu Ala Asn Gly Glu Ile Leu Ala Lys Arg Tyr Gly Gly Phe Met Lys Lys Asp Ala Glu Asp Asp Ser Leu Ala Asn Ser Ser Asp Leu Leu Lys Glu Leu Leu Glu Thr Gly Asp Asn Arg Glu Arg Ser His His Gln Asp Gly Ser AsnGlu Glu Glu Val Ser Lys Arg Tyr Gly Gly Phe Met Arg Gly Lys Arg Ser Pro Gln Leu Glu Asp Glu Ala Lys Glu Leu Gln Lys 2Tyr Gly Gly Phe Met Arg Arg Val Gly Arg Pro Glu Trp Trp Met 222yr Gln Lys Arg Tyr Gly GlyPhe Leu Lys Arg Phe Ala Glu Ala 225 234ro Ser Asp Glu Glu Gly Glu Ser Tyr Ser Lys Glu Val Pro Glu 245 25et Glu Lys Arg Tyr Gly Gly Phe Met Arg Phe 26lt;2SEQ ID NO 32LENGTH: 267 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Pro Arg Ser Cys Cys Ser Arg Ser Gly Ala Leu Leu Leu Ala Leu Leu Gln Ala Ser Met Glu Val Arg Gly Trp Cys Leu Glu Ser Ser 2 Gln Cys Gln Asp Leu Thr Thr Glu Ser Asn Leu Leu Glu Cys Ile Arg 35 4a Cys Lys Pro Asp Leu Ser Ala Glu Thr Pro Met Phe Pro Gly Asn 5 Gly Asp Glu Gln Pro Leu Thr Glu AsnPro Arg Lys Tyr Val Met Gly 65 7 His Phe Arg Trp Asp Arg Phe Gly Arg Arg Asn Ser Ser Ser Ser Gly 85 9r Ser Gly Ala Gly Gln Lys Arg Glu Asp Val Ser Ala Gly Glu Asp Gly Pro Leu Pro Glu Gly Gly Pro Glu Pro Arg Ser Asp Gly Ala Pro Gly Pro Arg Glu Gly Lys Arg Ser Tyr Ser Met Glu His Phe Trp Gly Lys Pro Val Gly Lys Lys Arg Arg Pro Val Lys Val Tyr Pro Asn Gly Ala Glu Asp Glu Ser Ala Glu Ala Phe Pro Leu Glu Phe ArgGlu Leu Thr Gly Gln Arg Leu Arg Glu Gly Asp Gly Pro Asp Pro Ala Asp Asp Gly Ala Gly Ala Gln Ala Asp Leu Glu His Ser 2Leu Val Ala Ala Glu Lys Lys Asp Glu Gly Pro Tyr Arg Met Glu 222he Arg Trp Gly Ser Pro ProLys Asp Lys Arg Tyr Gly Gly Phe 225 234hr Ser Glu Lys Ser Gln Thr Pro Leu Val Thr Leu Phe Lys Asn 245 25la Ile Ile Lys Asn Ala Tyr Lys Lys Gly Glu 26lt;2SEQ ID NO 32LENGTH: 236 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Pro Arg Ser Cys Cys Ser Arg Ser Gly Ala Leu Leu Leu Ala Leu Leu Gln Ala Ser Met Glu Val Arg Gly Trp Cys Leu Glu Ser Ser 2 Gln Cys Gln Asp Leu Thr Thr Glu Ser Asn Leu Leu Glu Cys Ile Arg 35 4a Cys Lys Pro Asp Leu Ser Ala Glu Thr Pro Met Phe Pro Gly Asn 5 Gly Asp Glu Gln Pro Leu Thr Glu AsnPro Arg Lys Tyr Val Met Gly 65 7 His Phe Arg Trp Asp Arg Phe Gly Arg Arg Asn Ser Ser Ser Ser Gly 85 9r Ser Gly Ala Gly Gln Lys Arg Glu Asp Val Ser Ala Gly Glu Asp Gly Pro Leu Pro Glu Gly Gly Pro Glu Pro Arg Ser Asp Gly Ala Pro Gly Pro Arg Glu Gly Lys Arg Ser Tyr Ser Met Glu His Phe Trp Gly Lys Pro Val Gly Lys Lys Arg Arg Pro Val Lys Val Tyr Pro Asn Gly Ala Glu Asp Glu Ser Ala Glu Ala Phe Pro Leu Glu Phe ArgGlu Leu Thr Gly Gln Arg Leu Arg Glu Gly Asp Gly Pro Asp Pro Ala Asp Asp Gly Ala Gly Ala Gln Ala Asp Leu Glu His Ser 2Leu Val Ala Ala Glu Lys Lys Asp Glu Gly Pro Tyr Arg Met Glu 222he Arg Trp Gly Ser Pro ProLys Asp Lys Arg 225 23lt;2SEQ ID NO 32LENGTH: 7 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 3Leu Pro Ser Pro Leu Phe ;2SEQ ID NO 32LENGTH: 8 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 3 Phe Leu Pro Ser Ser Pro Leu Phe ;2SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 3Phe Leu Pro SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 3Leu Phe Pro SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Pro Ser Ala SEQ ID NO 34SEQUENCE: 3<2SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Phe Leu Pro SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Leu Pro Phe SEQ ID NO 32LENGTH: 4 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Pro Leu Phe SEQ ID NO 32LENGTH: 4<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Pro Ser Pro SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Leu Val Ser SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Leu Phe Pro SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Leu Phe Ser SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 3Phe Ser Phe SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 3Phe Thr Ser SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 3Ser Leu Phe SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 32er Ser Phe SEQ ID NO 32LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 32hr Pro Ser SEQ ID NO 322 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <2SEQ ID NO 323 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE:323 Leu Pro Ser Phe SEQ ID NO 324 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 324 Phe Lys Pro Ser SEQ ID NO 325 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 325 Phe Leu Ser Pro SEQ ID NO 326 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 326 Phe Pro Leu Ser SEQ ID NO 327 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 327 Phe Pro Ser Leu SEQ ID NO 328 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 328 Phe Ser Pro Leu SEQ ID NO 329 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 329 Phe Ser Leu Pro SEQ ID NO 33LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 33he Pro Ser SEQ ID NO 33LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 33he Ser Pro SEQ ID NO 332 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 332 Leu Pro Phe Ser SEQ ID NO 333 <2LENGTH: 4 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 333 Leu Ser Pro Phe SEQ ID NO 334 <2LENGTH: 4<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 334 Leu Ser Phe Pro SEQ ID NO 335<2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 335 Pro Phe Leu Ser SEQ ID NO 336 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 336 Pro Phe Ser Leu SEQ ID NO 337 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 337 ProLeu Ser Phe SEQ ID NO 338 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 338 Pro Leu Phe Ser SEQ ID NO 339 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 339 Pro Ser Phe Leu SEQ ID NO 34LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide<4SEQUENCE: 34he Leu Pro SEQ ID NO 34LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Syntheticpolypeptide <4SEQUENCE: 34he Pro Leu SEQ ID NO 342 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of ArtificialSequence: Synthetic polypeptide <4SEQUENCE: 342 Ser Pro Phe Leu SEQ ID NO 343 <2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description ofArtificial Sequence: Synthetic polypeptide <4SEQUENCE: 343 Ser Leu Pro Phe SEQ ID NO 344 <2LENGTH: 3 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION:Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 344 Phe Leu Pro SEQ ID NO 345 <2LENGTH: 3 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHERINFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 345 Phe Pro Leu SEQ ID NO 346 <2LENGTH: 3 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 346 Pro Leu Phe SEQ ID NO 347 <2LENGTH: 3 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 347 Leu Pro Phe SEQ ID NO 348 <2LENGTH: 3 <2TYPE: PRT <2ORGANISM: Artificial Sequence<22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 348 Leu Phe Pro SEQ ID NO 349 <2LENGTH: 3 <2TYPE: PRT <2ORGANISM: ArtificialSequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 349 Pro Phe Leu SEQ ID NO 35LENGTH: 4 <2TYPE: PRT <2ORGANISM:Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 35eu Pro Ser SEQ ID NO 35LENGTH: 4 <2TYPE: PRT<2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 35eu Pro Ser SEQ ID NO 352 <2LENGTH: 4<2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 352 Ser Pro Leu Tyr SEQ ID NO 353<2LENGTH: 4 <2TYPE: PRT <2ORGANISM: Artificial Sequence <22EATURE: OTHER INFORMATION: Description of Artificial Sequence: Synthetic polypeptide <4SEQUENCE: 353 Ser Pro Leu Trp Other References
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